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Biopsy Punches, Sterile, 3.5 mm, Yellow

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Biopsy Punches, Sterile, 3.5 mm, Yellow FDA UDI
Generic Name
Skin-coring punch, single-use FDA UDI
Device Name
STERILE-R FDA UDI
Model / Reference
4090 FDA UDI
Description
STERILE-R FDA UDI

Identifiers

Primary DI / UDI-DI
00840117340725 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Skin-coring punch, single-use

Biopsy Punches, Sterile, 3.5 mm, Yellow by Dynarex Corp. — 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

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 2a3607a6-49c2-4c60-88a0-e7e9f4862159 33 fields · synced May 30, 2026