Evidence centre
Certificates and compliance documents
Review the legal entity, issuer, identifier, date, scope and model coverage printed in the documents supplied by Aurum Epoch. This evidence register separates organization-level certificates from product declarations, verification documents and report covers.
What this establishes
Traceable public evidence with its real limits.
Exact document identity
Each record shows the holder, issuer, document number, date and scope as printed in the supplied file.
Scope before badges
Organization certificates, product declarations, sample verifications and report covers are labelled separately.
Buyer verification route
Open the original file and confirm the exact model, configuration, classification, market and current status before an order.
Organization-level evidence
Quality-system certificates
These documents name Aurum Epoch Technology Co., Ltd. as the certificate holder or manufacturer and state the organization-level scope shown below.
View source Quality management system certificate
EN ISO 13485:2016 quality management system certificate
TÜV SÜD certificate for the quality management system and the medical laser/light-system scope printed on the certificate.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- TÜV SÜD Product Service GmbH
- Identifier
- Q5 091024 0004 Rev. 00
- Related record
- Report No. BJ1898304
- Issued
- Valid from
- Valid / stated until
Read exact scope
Scope: Design and development, manufacturing and distribution of Medical Intense Pulsed Light Therapy Systems, Medical Nd:YAG Laser Therapy Systems, Medical Diode Laser Therapy Systems and Medical Fractional CO2 Laser Therapy Systems.
Standards printed in the document:
- EN ISO 13485:2016
- ISO 13485:2016
- DIN EN ISO 13485:2016
Organization-level quality-management evidence. It does not by itself establish market authorization for every catalogue model.
View source EC full quality assurance system certificate
MDD EC Certificate — Full Quality Assurance System
TÜV SÜD EC certificate under Directive 93/42/EEC on Medical Devices (MDD), Annex II excluding section 4.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- TÜV SÜD Product Service GmbH (Notified Body 0123)
- Identifier
- G1 091024 0003 Rev. 03
- Related record
- Report No. BJ1998307
- Issued
- Valid from
- Valid / stated until
Read exact scope
Scope: Medical Nd:YAG Laser Therapy Systems, Medical Intense Pulsed Light Therapy Systems, Medical Fractional CO2 Laser Therapy Systems and Medical Diode Laser Therapy Systems. The certificate states that an additional Annex II (4) certificate is mandatory for marketing Class III devices.
The scope is limited to the product categories and quality-assurance system stated in the two-page certificate. Buyers should confirm the exact device, classification and destination-market requirements.
Product and test evidence
Declarations, verification and report cover
These records only apply to the product designation, model list and conditions printed in each source. They are not presented as interchangeable certificates.
View source Voluntary verification of conformity
Body Slimming & Skin Treatment System — voluntary conformity verification
ICR Polska document covering the named sample, directives, standards and model list printed in the document.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- ICR Polska Co. Ltd.
- Identifier
- ICR Polska/VC/HM220714
- Related record
- S/N 003043 · Test reports ENC2206306GZ92L1 and ENC2206306GZ92E1
- Issued
- Valid / stated until
Read exact scope and 26 named models
Scope: Body Slimming & Skin Treatment System; sample evaluation related to Directives 2014/35/EU and 2014/30/EU and the standards listed in the document.
Standards printed in the document:
- EN 60335-2-23:2003+A1:2008+A2:2015
- EN 60335-1:2012+A11:2014+A13:2017+A1:2019+A14:2019+A15:2021
- EN 62233:2008
- EN IEC 55014-1:2021
- EN IEC 55014-2:2021
- EN IEC 61000-3-2:2019+A1:2021
- EN 61000-3-3:2013+A1:2019+A2:2021
Models printed in the document:
Aurora-MED881, Aurora-MED887, Aurora-PHF711, Aurora-PHY13, Aurora-PVC541, Aurora-PVC778, Aurora-PVC809, Aurora-Silk073, Aurora-SKN443, Aurora-SKN-552, Aurora-SKN-933, Aurora-TNS151, Aurora-VCH1718, Aurora-VCH1892, Aurora-VM714, Vortex-Cro774, Vortex-Cro993, Vortex-EFP008, Vortex-ESV31, Vortex-ESV64, Vortex-PE5, Vortex-PE7, Vortex-PE9, Vortex-VLP6, Vortex-VLV1, Vortex-VLV3
The document expressly says it was issued on a voluntary basis and does not itself constitute a Notified Body conformity assessment or authorize use of the CE mark. It is therefore not presented here as a CE certificate.
View source RoHS product declaration
Laser Treatment System — RoHS product declaration
Product declaration image naming the applicant, manufacturer, product designation, covered models and referenced report.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- East Notice Certification Service Co., Ltd.
- Identifier
- ENC2306136GZ59
- Related record
- Report No. ENC2606136GZ59R1
- Issued
Read exact scope and 31 named models
Scope: Laser Treatment System; Commission Delegated Directive (EU) 2015/863 and (EU) 2017/2102 amending Annex II to Directive 2011/65/EU, subject to the surveillance and restrictions stated in the referenced report.
Models printed in the document:
Photon-PCF-034, Photon-PCF-091, Photon-PCF-718, Photon-VCF-213, Photon-VCF-431, Photon-VCF-762, Photon-PLD161, Photon-PLD171, Photon-PLD181, Photon-PLD191, Photon-VLD114, Photon-VLD452, Photon-VLD488, Photon-VLD658, Photon-VLD931, Photon-MID106, Photon-MID229, Photon-MID488, Photon-MPD809, Photon-MPD909, Photon-Dio142, Photon-Vio152, Photon-PNG110, Photon-VNG148, Photon-VNG248, Photon-VNG348, Photon-VNG448, Photon-RRS90, Photon-RS94, Photon-QH094, Photon-QH097
This is a supplied product-declaration image, not a batch COA. The document says it does not imply assessment of production and is applicable only to the equipment described.
View source RoHS product declaration
IPL & RF Treatment System — RoHS product declaration
Product declaration image naming the applicant, manufacturer, product designation, covered models and referenced report.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- East Notice Certification Service Co., Ltd.
- Identifier
- ENC2306136GZ63
- Related record
- Report No. ENC2606136GZ63R1
- Issued
Read exact scope and 17 named models
Scope: IPL & RF Treatment System; Commission Delegated Directive (EU) 2015/863 and (EU) 2017/2102 amending Annex II to Directive 2011/65/EU, subject to the surveillance and restrictions stated in the referenced report.
Models printed in the document:
Photon-Dio142, Photon-Vio152, Aurora-MED881, Aurora-MED887, Aurora-PHF711, Aurora-PHY13, Aurora-PVC541, Aurora-PVC778, Aurora-PVC809, Aurora-Silk073, Aurora-SKN443, Aurora-SKN-552, Aurora-SKN-933, Aurora-TNS151, Aurora-VCH1718, Aurora-VCH1892, Aurora-VM714
This is a supplied product-declaration image, not a batch COA. The document says it does not imply assessment of production and is applicable only to the equipment described.
View source Test report cover
Pathology Slide Printer — Low Voltage Directive test report cover
Cover image for a Low Voltage Directive test report supplied for the named Pathology Slide Printer models.
- Holder
- Aurum Epoch Technology Co., Ltd.
- Issuer
- East Notice Certification Service Co., Ltd.
- Identifier
- ENC2101180GZ49L1
- Issued
Read exact scope and 8 named models
Scope: Pathology Slide Printer models named on the supplied report cover.
Models printed in the document:
Photon-PCF034, Photon-VCF213, Photon-PLD161, Photon-VLD114, Photon-MID106, Photon-MPD809, Photon-VNG148, Photon-PHG110
Only the report cover was supplied. It is displayed as a report cover and is not represented as a complete test report, certificate, product approval or COA.
COA status
No Certificate of Analysis was supplied in this evidence set.
A COA is normally tied to a specific product or production batch and reports defined tests, methods, results and acceptance criteria. The supplied ISO 13485 certificate, EC quality-system certificate, RoHS declarations, voluntary conformity verification and test-report cover are different document types, so none has been relabelled as a COA.
If your procurement file requires a COA, identify the exact model, batch, destination market and required test basis in the quotation request.
Request model-specific documentsDocument FAQ
How to read and use this evidence.
Does one certificate cover every Aurum Epoch product?
No. Each document has its own holder, product category or model list, standard, validity and market context. Buyers should match the exact model and supplied configuration to the applicable current document.
Is the ICR document a CE certificate?
No. The document describes itself as a voluntary verification of conformity and states that it does not itself constitute a Notified Body conformity assessment or authorize the CE mark.
Are the RoHS documents batch certificates?
No. They are product declarations for the model lists printed in the supplied images. They are not Certificates of Analysis and do not identify a production batch.
Can Aurum Epoch provide a COA?
No batch-specific Certificate of Analysis was included in the evidence supplied for this page. If a buyer requires a COA or other batch record, the exact document, batch, model and test basis must be confirmed during the quotation and quality-document review.
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