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Boa Vision Ef

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
BOA VISION EF FDA UDI
Generic Name
Flexible video ureterorenoscope, reusable FDA UDI
Device Name
SENSOR-URETERORENOSCOPE 8.7FR WL 680MM flexible, working channel 3.6Fr, slanted distal tip Ø 6.6Fr, TL 980mm, deflection +270°/-270°, two function buttons, for connection to ENDOCAM Flex HD, LED-illumination, distal Sensor, Fixfocus FDA UDI
Model / Reference
73551071 FDA UDI
Description
SENSOR-URETERORENOSCOPE 8.7FR WL 680MM flexible, working channel 3.6Fr, slanted distal tip Ø 6.6Fr, TL 980mm, deflection +270°/-270°, two function buttons, for connection to ENDOCAM Flex HD, LED-illumination, distal Sensor, Fixfocus FDA UDI

Identifiers

Catalog Number
73551071 FDA UDI
Primary DI / UDI-DI
04055207054925 FDA UDI
FDA Product Code
FGB FDA UDI
FGA FDA UDI
GMDN Term
Flexible video ureterorenoscope, 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI

Dimensions & Sizes

Size
Length — 680 Millimeter FDA UDI
Outer Diameter — 2.9 Millimeter FDA UDI

Boa Vision Ef 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 485bad4a-9b54-48a1-99d2-0167d399be54 37 fields · synced Jun 6, 2026