← Back to catalogue

Extraction Tightening Assembly

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2027-12C

by Innomed, Inc.

Identity

Trade Name
Extraction Tightening Assembly EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Extractor EUDAMED
Extraction Tightening Assembly FDA UDI
Model / Reference
2027-12C EUDAMEDFDA UDI
Description
Extraction Tightening Assembly FDA UDI

Identifiers

Catalog Number
2027-12C FDA UDI
Primary DI / UDI-DI
00840277130235 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOEXTRACT0188 EUDAMED
Direct Marketing DI
00840277130235 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

Extraction Tightening Assembly 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED cf0cadec-3bfc-4724-aee6-9b5327e03609 61 fields · synced Jun 18, 2026
  • FDA UDI a758fab1-a05a-45f2-b52f-9ea82eaabe3e 34 fields · synced May 30, 2026