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Touch CMC 1 - Touch INTL rack

FDA UDIEUDAMED

Class III (US FDA UDI)

Ref SPD12AF01PN1APRef SPD12AF03RK1AP

by Keri Medical SA

Identity

Trade Name
TOUCH INTL tray EUDAMED
TOUCH INTL rack EUDAMED
Touch CMC 1 - Touch INTL rack FDA UDI
Touch CMC 1 - Metacarpal INTL rack FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Touch lid, Touch tray EUDAMED
Model / Reference
SPD12AF01PN1AP EUDAMEDFDA UDI
SPD12AF03RK1AP EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07640181162895 EUDAMEDFDA UDI
07640181162482 EUDAMEDFDA UDI
07640181162468 EUDAMED
Basic UDI-DI
764018116001AU EUDAMED
Direct Marketing DI
07640181162468 EUDAMED
07640181162895 EUDAMED
07640181162482 EUDAMED
PMA Number
P240020 FDA UDI
FDA Product Code
SFA FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class III FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

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 - Touch INTL rack 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 (5)

  • FDA UDI dd52d806-e699-4864-a6e7-bc71aa76ac04 33 fields · synced Aug 5, 2026
  • FDA UDI 69547532-d294-416e-9b01-d9b2851635f4 33 fields · synced May 30, 2026
  • EUDAMED a8df96be-e5bb-4b12-9995-22e6a0f0a32a 61 fields · synced Jun 19, 2026
  • EUDAMED ab91277a-16bc-40b8-91a1-9cdd74ce50ed 61 fields · synced Jul 15, 2026
  • EUDAMED 8c5eb895-dc44-44c2-938b-ebbc40351ed3 61 fields · synced Aug 5, 2026