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Rescue Single-use Grasping Forceps
EUDAMEDFDA UDIClass I (EU MDR)
Ref M00538350Model M00527750
Identity
- Trade Name
- Rescue Single-use Grasping Forceps EUDAMEDRescue FDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- Rescue Single-use Grasping Forceps EUDAMEDRescue Single Use Grasping Forceps FDA UDI
- Model / Reference
- M00527750 EUDAMEDM00538350 EUDAMEDFDA UDI
- Description
- Rescue Single Use Grasping Forceps FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16948318903983 EUDAMEDFDA UDI
- Basic UDI-DI
- 692683981s009SD EUDAMED
- Direct Marketing DI
- 16948318903983 EUDAMED
- 510(k) Number
- K101298 FDA UDI
- FDA Product Code
- OCZ FDA UDI
- EMDN Code
- G03080199 GASTROINTESTINAL ENDOSCOPY, FORCEPS, SINGLE-USE - 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
- 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
No
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
Yes
FDA UDI
Ethylene Oxide FDA UDI
Rescue 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 | 692683981s009SD | 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 1dff3cf2-ea66-49fc-b180-69487f747520 61 fields · synced Jul 18, 2026
- FDA UDI 8a562b9a-bcb1-4bf2-ba87-f10a35e3d271 34 fields · synced May 30, 2026