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Gauthier Biomedical

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5161-00-5023

by Gauthier Biomedical, Inc.

Identity

Trade Name
GAUTHIER BIOMEDICAL EUDAMEDFDA UDI
Generic Name
Manual orthopaedic bender, reusable FDA UDI
Device Name
CORONAL BENDER 6,0, LEFT EUDAMED
CORONAL BENDER 6.0, LEFT FDA UDI
Model / Reference
5161-00-5023 EUDAMED
5161-00-5023 (GC155006-20) FDA UDI
Description
CORONAL BENDER 6.0, LEFT FDA UDI

Identifiers

Catalog Number
5161005023 FDA UDI
Primary DI / UDI-DI
00858325005596 EUDAMEDFDA UDI
Basic UDI-DI
008583250055161-00-5023Q3 EUDAMED
Direct Marketing DI
00858325005596 EUDAMED
FDA Product Code
HXW FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Manual orthopaedic bender, reusable 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

No

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 ab0e3584-2279-4782-8f60-61b19568a17a 61 fields · synced Jun 8, 2026
  • FDA UDI bf5e4532-f39a-460d-b446-2416ed04bc84 35 fields · synced May 30, 2026