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Seesheen
EUDAMEDClass IIa (EU MDR)
Ref BR-GP13HT plusModel BR-GP13PF、BR-GP13PF plus、BR-GP13F 、BR-GP13F plus、BR-GP13PT 、BR-GP13PT plus、BR-GP13H 、BR-GP13H plus、BR-GP13HT、BR-GP13HT plus、BR-GP13HTB、BR-GP13HTB plus、BR-GP13TB、BR-GP13TB plus
Identity
- Trade Name
- SEESHEEN EUDAMED
- Device Name
- Flexible Video Bronchoscope EUDAMED
- Model / Reference
- BR-GP13PF、BR-GP13PF plus、BR-GP13F 、BR-GP13F plus、BR-GP13PT 、BR-GP13PT plus、BR-GP13H 、BR-GP13H plus、BR-GP13HT、BR-GP13HT plus、BR-GP13HTB、BR-GP13HTB plus、BR-GP13TB、BR-GP13TB plus EUDAMEDBR-GP13HT plus EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970680131001 EUDAMED
- Basic UDI-DI
- 69706801328BRBT EUDAMED
- Direct Marketing DI
- 06970680131001 EUDAMED
- EMDN Code
- Z12020802 VIDEO BRONCHOSCOPES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Seesheen by Zhuhai Seesheen Medical Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 69706801328BRBT | Class IIa | Active |
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Manufacturer
- Manufacturer
- Zhuhai Seesheen Medical Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000027274
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 8b170cf6-d475-40f5-be9a-8fda9eb8a0da 61 fields · synced Jun 18, 2026