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Enztec Classic OCI – Hex Driver

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 4252-2301

by Enztec Limited

Identity

Trade Name
OCI Hex Driver+ EUDAMEDFDA UDI
Enztec Classic OCI – Hex Driver FDA UDI
Generic Name
Orthopaedic implant impactor, reusable FDA UDI
Device Name
Enztec Cup Impactors EUDAMED
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
4252-2301 EUDAMEDFDA UDI
4252-2061 FDA UDI
Description
A reusable surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
4252-2061 FDA UDI
4252-2301 FDA UDI
Primary DI / UDI-DI
09421028116640 EUDAMEDFDA UDI
09421028111904 FDA UDI
Basic UDI-DI
942102811GMN00092B EUDAMED
Direct Marketing DI
09421028116640 EUDAMED
FDA Product Code
HWA FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS 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
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 implant impactor, reusable

Enztec Classic OCI – Hex Driver by Enztec Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, 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 (3)

  • FDA UDI b799ea81-8641-4f85-875e-823a4baed0a2 34 fields · synced Aug 4, 2026
  • FDA UDI 527e00ef-1958-4e32-8296-2ffe2a4257f1 34 fields · synced May 30, 2026
  • EUDAMED d0e4ea43-f0e4-46e3-8f89-19de3b794570 61 fields · synced Aug 4, 2026