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Touch CMC 1 - Bone Awl

FDA UDIEUDAMED

Class III (US FDA UDI)

Ref 000-A00900Ref 000-A01000

by Keri Medical SA

Identity

Trade Name
Bone Awl EUDAMEDFDA UDI
Touch CMC 1 - Bone Awl FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Reamers EUDAMED
Model / Reference
000-A00900 EUDAMEDFDA UDI
000-A01000 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07640181162826 EUDAMEDFDA UDI
07640181162246 EUDAMEDFDA UDI
Basic UDI-DI
764018116016B9 EUDAMED
Direct Marketing DI
07640181162826 EUDAMED
07640181162246 EUDAMED
PMA Number
P240020 FDA UDI
FDA Product Code
SFA FDA UDI
HWJ FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Class III FDA UDI
Regulation Number
888.4540 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

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 UDIFDA 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 UDIFDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDIFDA 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 - Bone Awl 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 (4)

  • FDA UDI f6360f9b-845e-4f8e-9a69-d43502725d98 33 fields · synced Jul 10, 2026
  • FDA UDI 12c41882-bae8-48a5-8d89-15fd44472e68 32 fields · synced May 30, 2026
  • EUDAMED f33fdd3c-e578-46d7-a8d9-ee8455c22a99 61 fields · synced Jul 9, 2026
  • EUDAMED c45a5f78-8624-4dcc-a39b-0616cee3846d 61 fields · synced Jul 10, 2026