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Single Use Grasping Forceps
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
Ref MD-C-GF2412
Identity
- Trade Name
- Single Use Grasping Forceps EUDAMEDFDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- Single Use Grasping forceps EUDAMEDwithout Plastic coated FDA UDI
- Model / Reference
- MD-C-GF2412 EUDAMEDFDA UDI
- Description
- without Plastic coated FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970401812080 EUDAMEDFDA UDI
- Basic UDI-DI
- 697040181GFCCoatR3 EUDAMED
- 510(k) Number
- K191900 FDA UDI
- FDA Product Code
- OCZ FDA UDI
- EMDN Code
- G03050199 DIGESTIVE ENDOSCOPY, RETRIEVAL DEVICES - OTHER 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
- Austria 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Single Use Grasping Forceps by Zhejiang Chuangxiang Medical Technology Co., Ltd. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K191900 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 697040181GFCCoatR3 | Class I | Active |
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Manufacturer
- Manufacturer
- Zhejiang Chuangxiang Medical Technology Co., LTD.
- EUDAMED SRN
- CN-MF-000012417
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (3)
- EUDAMED ad243f0e-5030-4bb7-81a6-025d8a083606 61 fields · synced Jul 26, 2026
- FDA UDI b0b0ef5d-946e-43fa-aa92-16f001f0c5f2 34 fields · synced May 30, 2026
- FDA 510(k) K191900 1 fields · synced May 18, 2026