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Polarcup Impactor Interface Sz 63

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 351342512163

by Enztec Limited

Identity

Trade Name
Polarcup Impactor Interface Sz 63 EUDAMEDFDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
Polarcup Instrumentation EUDAMED
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
351342512163 EUDAMEDFDA UDI
Description
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
351342512163 FDA UDI
Primary DI / UDI-DI
09421028114998 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN00272D EUDAMED
Direct Marketing DI
09421028114998 EUDAMED
FDA Product Code
HWA FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Netherlands 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

Polarcup Impactor Interface Sz 63 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

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Manufacturer

Manufacturer
Enztec Limited

Sources (2)

  • FDA UDI 75b17e78-de78-448d-bf4e-0d3881f3a5f1 34 fields · synced Jul 16, 2026
  • EUDAMED a3a642b9-6b28-42b3-ae02-60698e549525 61 fields · synced Jul 16, 2026