Instrapac

FDA UDI

Class I (US FDA UDI)

by Robinson Healthcare Limited

Identity

Trade Name: Instrapac FDA UDI
Generic Name: Open-surgery biopsy forceps, single-use FDA UDI
Device Name: Instrapac Schumacher Cervical Punch Biopsy Forceps 23cm X 10 FDA UDI
Model / Reference: 8259 FDA UDI
Description: Instrapac Schumacher Cervical Punch Biopsy Forceps 23cm X 10 FDA UDI

Identifiers

Catalog Number: 8259 FDA UDI
Primary DI / UDI-DI: 05010058082595 FDA UDI
FDA Product Code: HFB FDA UDI
GMDN Term: Open-surgery biopsy forceps, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4530 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 23 Centimeter FDA UDI

Category: Open-surgery biopsy forceps, single-use

Instrapac by Robinson Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Robinson Healthcare Limited

Sources (1)

FDA UDI 1639d422-ac80-4304-9f64-5e04a65e6039 37 fields · synced May 31, 2026