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Enztec Charnley - Fixed Blade Frame

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 4050-0151

by Enztec Limited

Identity

Trade Name
Enztec Charnley - Fixed Blade Frame EUDAMEDFDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Retractors and Frames EUDAMED
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
4050-0151 EUDAMEDFDA UDI
Description
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
4050-0151 FDA UDI
Primary DI / UDI-DI
09421028116862 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN003124 EUDAMED
Direct Marketing DI
09421028116862 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE EUDAMED
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
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

Yes

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

Category: Surgical retraction system, reusable

Enztec Charnley - Fixed Blade Frame by Enztec Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Enztec Limited

Sources (2)

  • FDA UDI 823ca0b7-cb6f-4760-bf4f-6e9dff800c20 34 fields · synced Jul 14, 2026
  • EUDAMED e1cb15d6-7460-450c-8a2c-f751882684bd 61 fields · synced Jul 14, 2026