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Tendon hook

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 265642Model TLS reusable instruments

by Fournitures Hospitalieres Industrie

Identity

Trade Name
Tendon hook EUDAMEDFDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
TLS reusable instruments EUDAMED
Model / Reference
265642 EUDAMEDFDA UDI
TLS reusable instruments EUDAMED

Identifiers

Primary DI / UDI-DI
03661489656422 EUDAMEDFDA UDI
Basic UDI-DI
3661489LIGTLSCIRMJZ EUDAMED
Direct Marketing DI
03661489656422 EUDAMED
510(k) Number
K113591 FDA UDI
K120740 FDA UDI
FDA Product Code
HWC FDA UDI
MBI FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3040 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

No

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 prosthesis implantation positioning instrument, reusable

Tendon hook by Fournitures Hospitalieres Industrie — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, 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

Sources (2)

  • FDA UDI e14ee84d-ba56-4eff-aba8-97c4039a311b 33 fields · synced Jun 19, 2026
  • EUDAMED 7fc34cdb-8983-4ef5-a9f5-97d3d02fc248 61 fields · synced Jun 19, 2026