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Modular Impactor Set

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5370

by Innomed, Inc.

Identity

Trade Name
Modular Impactor Set EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Orthopaedic implant impactor, reusable FDA UDI
Device Name
Impactor EUDAMED
Modular Impactor Set FDA UDI
Model / Reference
5370 EUDAMEDFDA UDI
Description
Modular Impactor Set FDA UDI

Identifiers

Catalog Number
5370 FDA UDI
Primary DI / UDI-DI
00840277111524 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOIMPACT01T2 EUDAMED
Direct Marketing DI
00840277111524 EUDAMED
FDA Product Code
HWA FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic implant impactor, 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

Modular Impactor Set 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 1620a514-a6e8-4aa5-af06-ea3aff03ab0f 61 fields · synced Jul 14, 2026
  • FDA UDI cbeab85c-933a-4285-b0f2-80f1369b444c 34 fields · synced May 30, 2026