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Harvey Lumbar Bone Graft Pusher

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5083-02

by Innomed, Inc.

Identity

Trade Name
Harvey Lumbar Bone Graft Pusher EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Bone graft funnel FDA UDI
Device Name
Guide EUDAMED
Harvey Lumbar Bone Graft Pusher FDA UDI
Model / Reference
5083-02 EUDAMEDFDA UDI
Description
Harvey Lumbar Bone Graft Pusher FDA UDI

Identifiers

Catalog Number
5083-02 FDA UDI
Primary DI / UDI-DI
00840277121615 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOGUIDE01VS EUDAMED
Direct Marketing DI
00840277121615 EUDAMED
FDA Product Code
FZX FDA UDI
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED
GMDN Term
Bone graft funnel 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

Harvey Lumbar Bone Graft Pusher 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

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Manufacturer

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

Sources (2)

  • EUDAMED 20c5bf02-e75d-49e4-bc9f-2d76c857ab89 61 fields · synced Jul 17, 2026
  • FDA UDI e1f973fd-7734-4c24-a58b-f400221e3ede 34 fields · synced May 30, 2026