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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 access cannula, reusable FDA UDI
Device Name
TROCAR SLEEVE STRAI. CAP 5.5MM WL 100MM stainless steel-sheath tube with thread, distal tip straight, with Magnet-ball valve, with insufflation valve, reusable FDA UDI
Model / Reference
8921024 FDA UDI
Description
TROCAR SLEEVE STRAI. CAP 5.5MM WL 100MM stainless steel-sheath tube with thread, distal tip straight, with Magnet-ball valve, with insufflation valve, reusable FDA UDI

Identifiers

Catalog Number
8921.024 FDA UDI
Primary DI / UDI-DI
04055207022146 FDA UDI
FDA Product Code
FBQ FDA UDI
GMDN Term
Laparoscopic access cannula, 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 — 100 Millimeter FDA UDI

Category: Laparoscopic access cannula, 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 access cannula, 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 68170ef0-67a3-48f5-a45a-9195f48761d3 36 fields · synced Jun 8, 2026