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Vertebris

FDA UDI

Class I (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
VERTEBRIS FDA UDI
Generic Name
Flexible endoscopic scissors, reusable FDA UDI
Device Name
SCISSORS Ø 3MM WL 360MM color code red, TL 457mm, with irrigation connection, reusable FDA UDI
Model / Reference
892401703 FDA UDI
Description
SCISSORS Ø 3MM WL 360MM color code red, TL 457mm, with irrigation connection, reusable FDA UDI

Identifiers

Catalog Number
89240.1703 FDA UDI
Primary DI / UDI-DI
04055207035504 FDA UDI
FDA Product Code
HRR FDA UDI
GMDN Term
Flexible endoscopic scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 360 Millimeter FDA UDI
Outer Diameter — 3 Millimeter FDA UDI

Category: Flexible endoscopic scissors, reusable

Vertebris by Richard Wolf GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic scissors, reusable.

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 bfddc75a-acb3-49fa-b9e0-f41c24e68a5e 36 fields · synced Jun 8, 2026