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E-Line

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
E-LINE FDA UDI
Generic Name
Pin-indexed adaptor, reusable FDA UDI
Device Name
ADAPTER FOR CYSTOSCOPE only for diagnostics, TL 79mm, compatible with sheaths 86520145, 86520245, 86520345, 86520445, and telescopes Ø 4mm, 0°/12°/30°/70°, without insertion port, bayonet-cap, reusable FDA UDI
Model / Reference
8652254 FDA UDI
Description
ADAPTER FOR CYSTOSCOPE only for diagnostics, TL 79mm, compatible with sheaths 86520145, 86520245, 86520345, 86520445, and telescopes Ø 4mm, 0°/12°/30°/70°, without insertion port, bayonet-cap, reusable FDA UDI

Identifiers

Catalog Number
8652.254 FDA UDI
Primary DI / UDI-DI
04055207018514 FDA UDI
FDA Product Code
FBO FDA UDI
GMDN Term
Pin-indexed adaptor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

E-Line by Richard Wolf GmbH — Class II — 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
Richard Wolf GmbH

Sources (1)

  • FDA UDI 17366212-8577-4b70-9783-8e755531329d 36 fields · synced May 30, 2026