Identity
- Trade Name
- Reicodent FDA UDI
- Generic Name
- Tooth extraction forceps FDA UDI
- Device Name
- Extracting Forceps EUDAMEDKIDS-EXTRACT - Extracting forceps # 22S Molars FDA UDI
- Model / Reference
- 02-500-22 S EUDAMEDFDA UDI
- Description
- KIDS-EXTRACT - Extracting forceps # 22S Molars FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04061644041671 EUDAMEDFDA UDI
- Basic UDI-DI
- 4061644PG0202CC EUDAMED
- Direct Marketing DI
- 04061644041671 EUDAMED
- FDA Product Code
- EMG FDA UDI
- EMDN Code
- L150301 DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Tooth extraction forceps FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Germany 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Tooth extraction forceps
Reicodent by devemed GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Tooth extraction forceps.
- TEKNO® — Tekno Medical Optik-Chirurgie GmbH & Co. · Class I
- Premier Forceps — PREMIER DENTAL PRODUCTS COMPANY · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- A. Titan Instruments — A.Titan Instruments · Class I
- Power Dental USA — Power Dental USA, Inc. · Class I
- CROWN SPLITTER ON LARGE T BAR — W.H. Holden, Inc. · Class I
- NORDENT MANUFACTURING INC — NORDENT MANUFACTURING INC · Class I
- ZOLL-DENTAL — Zoll-Dental · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- devemed GmbH
Sources (2)
- FDA UDI dda0e302-01e0-47ad-8e80-914bf07a5479 34 fields · synced Sep 17, 2026
- EUDAMED ab45d347-53c1-4a59-a891-a8c1268ce69b 61 fields · synced Sep 17, 2026