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O'Reilly Femoral Head Extractor Device

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3675

by Innomed, Inc.

Identity

Trade Name
O'Reilly Femoral Head Extractor Device EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Extractor EUDAMED
O'Reilly Femoral Haed Extractor Device FDA UDI
Model / Reference
3675 EUDAMEDFDA UDI
Description
O'Reilly Femoral Haed Extractor Device FDA UDI

Identifiers

Catalog Number
3675 FDA UDI
Primary DI / UDI-DI
00840277106117 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOEXTRACT0188 EUDAMED
Direct Marketing DI
00840277106117 EUDAMED
FDA Product Code
HWB FDA UDI
EMDN Code
L0921 NON-IMPLANTABLE ORTHOPAEDIC DEVICES EXTRACTORS, REUSABLE EUDAMED
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 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

O'Reilly Femoral Head Extractor Device 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 aebc39b4-14fa-4948-b48c-95eebc5f4670 61 fields · synced Jul 11, 2026
  • FDA UDI 8b9a6e56-ee35-4d66-b969-6a3a52759037 34 fields · synced May 30, 2026