← Back to catalogue

Arthroscopic adapters

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 89101.0000Model 10000201158

by Richard Wolf GmbH

Identity

Trade Name
ARTRHOLUTION FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Arthroscopic adapters EUDAMED
SEALING PART FOR SHEATH reusable FDA UDI
Model / Reference
10000201158 EUDAMED
89101.0000 EUDAMED
891010000 FDA UDI
Description
SEALING PART FOR SHEATH reusable FDA UDI

Identifiers

Catalog Number
89101.0000 FDA UDI
Primary DI / UDI-DI
04055207034125 EUDAMEDFDA UDI
Basic UDI-DI
405520722052019-0017805GA EUDAMED
Direct Marketing DI
04055207034125 EUDAMED
FDA Product Code
NBH FDA UDI
EMDN Code
A0799 ADAPTERS, CONNECTORS, RAMPS, STOPCOCKS, CAPS - OTHER EUDAMED
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.1100 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Arthroscopic adapters by Richard Wolf GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Richard Wolf GmbH
EUDAMED SRN
DE-MF-000007048

Sources (2)

  • EUDAMED 0b492d41-0d8e-4eba-960a-849bbe99c3ca 61 fields · synced Jun 17, 2026
  • FDA UDI cb1cdfc4-fd06-49cd-9fd4-6b568d7ec21e 36 fields · synced May 30, 2026