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ENDOZIME INSTRUSPONGE 4mm (FLEXIBLE)

FDA UDI

Class I (US FDA UDI)

by Ruhof Corporation

Identity

Trade Name
ENDOZIME INSTRUSPONGE 4mm (FLEXIBLE) FDA UDI
Generic Name
Semiconductor-type radiation survey meter FDA UDI
Device Name
brushes to clean medical instrumnets FDA UDI
Model / Reference
345ESS4F FDA UDI
Description
brushes to clean medical instrumnets FDA UDI

Identifiers

Primary DI / UDI-DI
00810929010147 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Semiconductor-type radiation survey meter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 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

Yes

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

No

FDA UDI

Category: Semiconductor-type radiation survey meter

ENDOZIME INSTRUSPONGE 4mm (FLEXIBLE) by Ruhof Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ruhof Corporation

Sources (1)

  • FDA UDI 10af3b0f-c05d-4624-b58d-063757060cb4 34 fields · synced May 31, 2026