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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
Rigid endoscope obturator FDA UDI
Device Name
OBTURATOR FOR CYSTOSCOPE 16FR color code yellow, WL 230mm, oval, rounded distal end, compatible with sheath 86520145, reusable FDA UDI
Model / Reference
86520147 FDA UDI
Description
OBTURATOR FOR CYSTOSCOPE 16FR color code yellow, WL 230mm, oval, rounded distal end, compatible with sheath 86520145, reusable FDA UDI

Identifiers

Catalog Number
8652.0147 FDA UDI
Primary DI / UDI-DI
04055207027967 FDA UDI
FDA Product Code
FBO FDA UDI
GMDN Term
Rigid endoscope obturator 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

Dimensions & Sizes

Size
Outer Diameter — 5.33333333333 Millimeter 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 86e729fb-2437-46cf-83f0-20007841faf5 37 fields · synced May 30, 2026