← Back to catalogue

Unity ASC - Ankle Clamp

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 1232152

by Enztec Limited

Identity

Trade Name
Unity ASC - Ankle Clamp EUDAMEDFDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
Tibial Alignment Guides EUDAMED
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
1232152 EUDAMEDFDA UDI
Description
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
1232152 FDA UDI
Primary DI / UDI-DI
09421028113038 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN003226 EUDAMED
Direct Marketing DI
09421028113038 EUDAMED
FDA Product Code
FZX FDA UDI
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
France 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

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: Orthopaedic prosthesis implantation positioning instrument, reusable

Unity ASC - Ankle Clamp by Enztec Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Enztec Limited

Sources (2)

  • FDA UDI b840a9ab-31df-45e2-b05f-bd93d238d0ac 34 fields · synced Jun 19, 2026
  • EUDAMED ec30c764-994e-4615-af7d-8acdf4663f98 61 fields · synced Jun 19, 2026