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Touch CMC 1 - Metacarpal Rasp 0

FDA UDIEUDAMED

Class III (US FDA UDI)

by Keri Medical SA

Identity

Trade Name
Touch CMC 1 - Metacarpal Rasp 0 FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Model / Reference
112-A31000 FDA UDI

Identifiers

Primary DI / UDI-DI
07640181161638 FDA UDI
PMA Number
P240020 FDA UDI
FDA Product Code
SFA FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Touch CMC 1 - Metacarpal Rasp 0 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.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keri Medical SA

Sources (2)

  • FDA UDI 9e15ce99-0ee5-4d26-a671-dd203c2760ac 33 fields · synced Jun 11, 2026
  • EUDAMED 1 fields · synced Jun 11, 2026