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Riwo-Art

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
RIWO-ART FDA UDI
Generic Name
Laparoscopic trocar blade, reusable FDA UDI
Device Name
TROCAR TIP TRIANGULAR SZ 5.5MM WL 169MM distal tip triangular, reusable FDA UDI
Model / Reference
8921123 FDA UDI
Description
TROCAR TIP TRIANGULAR SZ 5.5MM WL 169MM distal tip triangular, reusable FDA UDI

Identifiers

Catalog Number
8921.123 FDA UDI
Primary DI / UDI-DI
04055207044797 FDA UDI
FDA Product Code
FBQ FDA UDI
GMDN Term
Laparoscopic trocar blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5090 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 — 169 Millimeter FDA UDI

Category: Laparoscopic trocar blade, reusable

Riwo-Art by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic trocar blade, 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 3d984b62-ff03-482b-9e54-209d82166f71 36 fields · synced Jun 8, 2026