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VersaGrasp Single-Use Grasping Forceps
EUDAMEDFDA UDIClass I (EU MDR)
Ref M0067802000
Identity
- Trade Name
- VersaGrasp Single-Use Grasping Forceps EUDAMEDVersaGrasp Single use Grasping Forceps FDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- VersaGrasp Single-Use Grasping Forceps EUDAMEDVersaGrasp Single use Grasping Forceps FDA UDI
- Model / Reference
- M0067802000 EUDAMEDFDA UDI
- Description
- VersaGrasp Single use Grasping Forceps FDA UDI
Identifiers
- Catalog Number
- M0067802000 FDA UDI
- Primary DI / UDI-DI
- 06948318996797 EUDAMEDFDA UDI
- Basic UDI-DI
- 692683981s013S4 EUDAMED
- Direct Marketing DI
- 06948318996797 EUDAMED
- FDA Product Code
- PTS FDA UDI
- EMDN Code
- U09030102 EXTRACTION FORCEPS FOR UROGENITAL ENDOSCOPY, SINGLE-USE EUDAMED
- GMDN Term
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
VersaGrasp Single-Use Grasping Forceps by Anrei Medical (HZ) CO., LTD. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 692683981s013S4 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Anrei Medical (HZ) Co., Ltd.
- EUDAMED SRN
- CN-MF-000009964
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (2)
- EUDAMED ad843b9b-5fab-4092-afb9-931669e39ef4 61 fields · synced Jul 13, 2026
- FDA UDI b0c351fa-848b-4206-871d-5bddc876274a 34 fields · synced May 30, 2026