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Robbins True-Cut Disposable Biopsy Punches

FDA UDI

Class I (US FDA UDI)

by Robbins Instruments

Identity

Trade Name
Robbins True-Cut Disposable Biopsy Punches FDA UDI
Generic Name
Open-surgery biopsy forceps, single-use FDA UDI
Device Name
Disposable Biopsy Punch 2,3,3.5,4,5mm FDA UDI
Model / Reference
RBP-A FDA UDI
Description
Disposable Biopsy Punch 2,3,3.5,4,5mm FDA UDI

Identifiers

Catalog Number
RBP-A FDA UDI
Primary DI / UDI-DI
90850010779211 FDA UDI
FDA Product Code
LRY FDA UDI
GMDN Term
Open-surgery biopsy forceps, 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Open-surgery biopsy forceps, single-use

Robbins True-Cut Disposable Biopsy Punches by Robbins Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery biopsy forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Robbins Instruments

Sources (1)

  • FDA UDI c3d88825-d0d4-4a67-bd5d-0a3a300635ca 35 fields · synced Jun 1, 2026