← Back to catalogue

Burkhead Glenoid Retractor Solid Large

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5839

by Innomed, Inc.

Identity

Trade Name
Burkhead Glenoid Retractor Solid Large EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
Retractor EUDAMED
Burkhead Glenoid Retractor Solid Large FDA UDI
Model / Reference
5839 EUDAMEDFDA UDI
Description
Burkhead Glenoid Retractor Solid Large FDA UDI

Identifiers

Catalog Number
5839 FDA UDI
Primary DI / UDI-DI
00840277117878 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNORETRACT016A EUDAMED
Direct Marketing DI
00840277117878 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE EUDAMED
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Burkhead Glenoid Retractor Solid Large by Innomed, 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

Manufacturer
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 5d633b88-e250-4a77-915f-cd1995c9ac72 61 fields · synced Jul 12, 2026
  • FDA UDI 8723085c-1286-463c-8e48-f1ca402d02e2 34 fields · synced May 30, 2026