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Metal Hemi

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
METAL HEMI FDA UDI
Generic Name
Bone-coring punch, reusable FDA UDI
Device Name
Cruciate Punch FDA UDI
Model / Reference
03-6000-11 FDA UDI
Description
Cruciate Punch FDA UDI

Identifiers

Catalog Number
03-6000-11 FDA UDI
Primary DI / UDI-DI
00889797037884 FDA UDI
FDA Product Code
HWP FDA UDI
GMDN Term
Bone-coring punch, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-coring punch, reusable

A comprehensive 2-3 paragraph SEO description written in clear, natural language. This device is a hand-held manual surgical instrument designed to cut out (core) sections of bone, or a combination of bone and soft-tissue during surgery.

Similar devices

Also classified as Bone-coring punch, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wright Medical Technology, Inc.

Sources (1)

  • FDA UDI 6726fcd1-5bbf-4e4e-9df3-964d6e98be16 35 fields · synced Jul 25, 2026