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Enztec ORD – Open - Harris

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 4250-7100

by Enztec Limited

Identity

Trade Name
Enztec ORD - Open - Harris EUDAMED
Enztec ORD – Open - Harris FDA UDI
Generic Name
Surgical power tool adaptor FDA UDI
Device Name
Reamer Drivers and Acetabular Reamers EUDAMED
A surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
4250-7100 EUDAMEDFDA UDI
Description
A surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
4250-7100 FDA UDI
Primary DI / UDI-DI
09421028118293 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN003022 EUDAMED
Direct Marketing DI
09421028113274 EUDAMED
FDA Product Code
HWE FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical power tool adaptor FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4820 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 power tool adaptor

Enztec ORD – Open - Harris by Enztec Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool adaptor.

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 44a187e6-1134-4ef0-bfcf-ef911415bc0c 34 fields · synced Jul 28, 2026
  • EUDAMED 86e83875-d334-458c-9f14-2483640852b2 61 fields · synced Jul 28, 2026