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Exactech Straight DA Broach Handle

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 4251-4080

by Enztec Limited

Identity

Trade Name
Exactech Straight DA Broach Handle EUDAMEDFDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Broach Handles EUDAMED
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
4251-4080 EUDAMEDFDA UDI
Description
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
4251-4080 FDA UDI
Primary DI / UDI-DI
09421028116756 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN0002ZS EUDAMED
Direct Marketing DI
09421028116756 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Spain 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: Surgical instrument handle, non-torque-limiting

Exactech Straight DA Broach Handle by Enztec Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

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 3d419ed7-f69e-4f67-b5e1-61b5009b1133 34 fields · synced Jul 26, 2026
  • EUDAMED f8cf6410-f891-4325-9412-4a31ec556370 61 fields · synced Jul 26, 2026