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Cannulated conical reamer ⌀10 mm PLUS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 112-A22310Ref 112-A22110Ref 112-A21110

by Keri Medical SA

Identity

Trade Name
Cannulated conical reamer ⌀10 mm PLUS EUDAMED
Cannulated conical reamer ⌀ 10 mm EUDAMED
Conical reamer ⌀ 10 mm EUDAMED
Touch CMC 1 - Cannulated Conical Reamer Ø10 FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Reamers EUDAMED
Model / Reference
112-A22310 EUDAMED
112-A22110 EUDAMEDFDA UDI
112-A21110 EUDAMED

Identifiers

Primary DI / UDI-DI
07640181163052 EUDAMED
07640181161218 EUDAMEDFDA UDI
07640181161171 EUDAMED
Basic UDI-DI
764018116016B9 EUDAMED
PMA Number
P240020 FDA UDI
FDA Product Code
SFA 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 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

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

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

Cannulated conical reamer ⌀10 mm PLUS by Keri Medical SA — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keri Medical SA
EUDAMED SRN
CH-MF-000021960
Authorised Representative
Keri Medical France FR-AR-000009590

Sources (4)

  • EUDAMED 59d7d17b-e404-444f-9032-cb4d06b5e79a 61 fields · synced Oct 6, 2026
  • FDA UDI 8c8f9447-0805-48d0-9eb9-a14323812102 33 fields · synced May 30, 2026
  • EUDAMED 8083dbcf-bb63-4de2-b19c-09cbd24a16d8 61 fields · synced Jul 31, 2026
  • EUDAMED e91f512d-2685-4adb-b120-cd0656ecb77a 61 fields · synced Sep 18, 2026