Identity
- Trade Name
- Dental Instrument EUDAMEDFDA UDIRest Plate EUDAMED
- Generic Name
- Screw extractor, single-use FDA UDI
- Device Name
- Rest Plate EUDAMEDCOWELL® Reusable Surgical Instrument EUDAMED
- Model / Reference
- KARP001B EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800016105643 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08800016105643 EUDAMED880947172M01RED04T07XX EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- L80 SURGICAL INSTRUMENTS, REUSABLE - VARIOUS ACCESSORIES EUDAMED
- GMDN Term
- Screw extractor, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dental Instrument by Cowellmedi Co., Ltd — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-08800016105643 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-08800016105643 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Cowellmedi Co., Ltd.
- EUDAMED SRN
- KR-MF-000009689
- Authorised Representative
- AR Experts B.V. NL-AR-000023989
Sources (3)
- EUDAMED 7a57b56b-0532-426f-b34c-9636204e5b51 61 fields · synced Jul 17, 2026
- FDA UDI 236973b2-b8bc-4a18-935d-981b30c9b9f8 32 fields · synced May 30, 2026
- EUDAMED 62c8f040-deec-4c73-83a7-eb2000aaf4ff 61 fields · synced Jul 8, 2026