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Gauthier Biomedical

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5161-00-5047

by Gauthier Biomedical, Inc.

Identity

Trade Name
GAUTHIER BIOMEDICAL EUDAMEDFDA UDI
Generic Name
Surgical instrument handle, torque-limiting FDA UDI
Device Name
TORQUE LIMITER, 11,3 NM EUDAMED
TORQUE LIMITER, 11.3NM FDA UDI
Model / Reference
5161-00-5047 EUDAMED
5161-00-5047(G919508) FDA UDI
Description
TORQUE LIMITER, 11.3NM FDA UDI

Identifiers

Catalog Number
5161005047 FDA UDI
Primary DI / UDI-DI
00858325005671 EUDAMEDFDA UDI
Basic UDI-DI
008583250055161-00-5047QH EUDAMED
Direct Marketing DI
00858325005671 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical instrument handle, torque-limiting FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Gauthier Biomedical by Gauthier Biomedical, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000015766
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED ca6f6382-304b-4c34-b9a9-d71aaeb98f31 61 fields · synced Jul 10, 2026
  • FDA UDI d0c283b5-8392-4350-a1d4-63cf36031de7 35 fields · synced May 30, 2026