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Integra® Miltex®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Miltex® FDA UDI
Generic Name
Skin-coring punch, single-use FDA UDI
Device Name
Integra® Miltex® Disposable Biopsy Punch 5.0mm FDA UDI
Model / Reference
33-35 FDA UDI
Description
Integra® Miltex® Disposable Biopsy Punch 5.0mm FDA UDI

Identifiers

Catalog Number
33-35 FDA UDI
Primary DI / UDI-DI
10381780064121 FDA UDI
FDA Product Code
LRY FDA UDI
GMDN Term
Skin-coring punch, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-coring punch, single-use

Integra® Miltex® by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-coring punch, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 330d0767-4152-4112-a601-871beb24ded9 35 fields · synced Jun 9, 2026