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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
End-cut biopsy gun handpiece/needle FDA UDI
Device Name
BIOPSY PUNCH,STERILE,DISP,1MM,50/BX FDA UDI
Model / Reference
MDS0033310B FDA UDI
Description
BIOPSY PUNCH,STERILE,DISP,1MM,50/BX FDA UDI

Identifiers

Catalog Number
MDS0033310B FDA UDI
Primary DI / UDI-DI
20193489141235 FDA UDI
FDA Product Code
EME FDA UDI
GMDN Term
End-cut biopsy gun handpiece/needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: End-cut biopsy gun handpiece/needle

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as End-cut biopsy gun handpiece/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d69e279b-3b18-41fb-ac13-c1a9f9c51f67 36 fields · synced May 30, 2026