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Retractor ME-EC0002

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ME-EC0002

by Innomed, Inc.

Identity

Trade Name
Retractor ME-EC0002 EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
Retractor EUDAMED
Retractor ME-EC0002 FDA UDI
Model / Reference
ME-EC0002 EUDAMEDFDA UDI
Description
Retractor ME-EC0002 FDA UDI

Identifiers

Catalog Number
ME-EC0002 FDA UDI
Primary DI / UDI-DI
00840277124326 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNORETRACT016A EUDAMED
Direct Marketing DI
00840277124326 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

Retractor ME-EC0002 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 c709eb86-adb6-42e1-9ef3-bb2d383a3b43 61 fields · synced Sep 17, 2026
  • FDA UDI 56e51cda-d59f-49ee-9873-9d8889080478 34 fields · synced May 30, 2026