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Cup Removal Starter Instrument - 56mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5200-56

by Innomed, Inc.

Identity

Trade Name
Cup Removal Starter Instrument - 56mm EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Extractor EUDAMED
Cup Removal Starter Instrument 56mm FDA UDI
Model / Reference
5200-56 EUDAMEDFDA UDI
Description
Cup Removal Starter Instrument 56mm FDA UDI

Identifiers

Catalog Number
5200-56 FDA UDI
Primary DI / UDI-DI
00840277104014 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOEXTRACT0188 EUDAMED
Direct Marketing DI
00840277104014 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

Cup Removal Starter Instrument - 56mm 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 996de03a-acdb-4b83-8786-12e97f3db25c 61 fields · synced Jun 17, 2026
  • FDA UDI 667f58f9-3c3e-4a71-be8a-34b1e858f96a 34 fields · synced May 30, 2026