← Back to catalogue

Arthroline

FDA UDI

Class I (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
ARTHROLINE FDA UDI
Generic Name
Rigid endoscopic scissors, reusable FDA UDI
Device Name
SCISSORS PUNCH W 2.4MM H 2.1MM jaw straight, sheath straight, WL 120 mm, reusable FDA UDI
Model / Reference
891400505 FDA UDI
Description
SCISSORS PUNCH W 2.4MM H 2.1MM jaw straight, sheath straight, WL 120 mm, reusable FDA UDI

Identifiers

Catalog Number
89140.0505 FDA UDI
Primary DI / UDI-DI
04055207046364 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Rigid endoscopic scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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
Width — 2.4 Millimeter FDA UDI
Height — 2.1 Millimeter FDA UDI

Category: Rigid endoscopic scissors, reusable

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

Similar devices

Also classified as Rigid endoscopic scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI ab87a3d1-bd43-49e9-9456-3045a55b5220 37 fields · synced May 30, 2026