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Crocodile Micro Forceps, steel finish
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref CF2001-SModel Forceps
Identity
- Trade Name
- Crocodile Micro Forceps, steel finish EUDAMEDFDA UDI
- Generic Name
- ENT foreign body extraction forceps FDA UDI
- Model / Reference
- Forceps EUDAMEDCF2001-S EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060212050953 EUDAMEDFDA UDI
- Basic UDI-DI
- 506021205TF24XE EUDAMED
- FDA Product Code
- KAE FDA UDI
- EMDN Code
- Q030304 ENT SURGERY FORCEPS, SINGLE-USE EUDAMED
- GMDN Term
- ENT foreign body extraction forceps FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Market of Registration
- Netherlands 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
Yes
FDA UDI
Crocodile Micro Forceps, steel finish by Dtr Medical Ltd — Class IIa — 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 | 506021205TF24XE | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Dtr Medical Ltd
- EUDAMED SRN
- GB-MF-000023112
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED f675eb7c-1523-4a26-bbcc-291c84bd9d8e 61 fields · synced Jun 18, 2026
- FDA UDI 0bc3fc32-bb9d-471c-9e82-a50219a42806 32 fields · synced May 30, 2026