Hysafe

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name: HYSAFE FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: GRASP.FORCEPS INSERT 10.5FR WL 340MM WL 350mm, double action, take-apart, reusable FDA UDI
Model / Reference: 86426008 FDA UDI
Description: GRASP.FORCEPS INSERT 10.5FR WL 340MM WL 350mm, double action, take-apart, reusable FDA UDI

Identifiers

Catalog Number: 8642.6008 FDA UDI
Primary DI / UDI-DI: 04055207027776 FDA UDI
FDA Product Code: OCZ FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 3.5 Millimeter FDA UDI
Length — 340 Millimeter FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

Hysafe by Richard Wolf GmbH — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Richard Wolf GmbH

Sources (1)

FDA UDI 1de1ba32-2f24-48dc-b9f8-ad55d324d997 36 fields · synced Jun 1, 2026