Touch CMC 1 - Metacarpal Rasp 4
FDA UDIEUDAMEDClass III (US FDA UDI)
Identity
- Trade Name
- Metacarpal rasp 4 EUDAMEDTouch CMC 1 - Metacarpal Rasp 4 FDA UDI
- Generic Name
- Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- Rasps EUDAMED
- Model / Reference
- 112-A31004 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 07640181160983 EUDAMED07640181161676 FDA UDI
- Basic UDI-DI
- 764018116014B5 EUDAMED
- Direct Marketing DI
- 07640181160983 EUDAMED
- PMA Number
- P240020 FDA UDI
- FDA Product Code
- SFA FDA UDI
- EMDN Code
- L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass III FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Orthopaedic surgical procedure kit, non-medicated, reusable
Touch CMC 1 - Metacarpal Rasp 4 by Keri Medical SA — Class III — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.
- Knee Instruments — Medacta International · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Spine Instruments — Medacta International · Class I
- Knee Instruments — Medacta International · Class I
- RAZEK EQUIPAMENTOS — RAZEK EQUIPAMENTOS LTDA · Class I
- General Instruments — ORTHOPEDIATRICS CORP. · Class I
- Hip Instruments — Medacta International · Class I
- ORTHOPEDIC MANUAL SURGICAL INSTRUMENT — FX SOLUTIONS · Class I
Cleared under the same submission
P240020 also covers:
- TOUCH® CMC 1 — Keri Medical SA
- TOUCH® CMC 1 — Keri Medical SA
- TOUCH® CMC 1 — Keri Medical SA
- TOUCH® CMC 1 — Keri Medical SA
- Touch CMC 1 - Bone Awl — Keri Medical SA
- Touch CMC 1 - Cannulated Conical Reamer Ø9 — Keri Medical SA
- Touch CMC 1 - Cannulated Trapezium Starter — Keri Medical SA
- Touch CMC 1 - Kirschner wire — Keri Medical SA
- Touch CMC 1 - Kirschner wire Tube 16 cm Ø12mm — Keri Medical SA
- Touch CMC 1 - Metacarpal INTL rack lid — Keri Medical SA
- Touch CMC 1 - Metacarpal Rasp 0 — Keri Medical SA
- Touch CMC 1 - Metacarpal Rasp 1 — Keri Medical SA
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class III | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Keri Medical SA
Sources (2)
- FDA UDI c2b7a3b2-a177-495a-84f7-c176f6648a0f 33 fields · synced Jul 10, 2026
- EUDAMED 05cb604f-c0c4-423b-a7c5-4ca0fc041e5c 61 fields · synced Jul 10, 2026