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Suction tube set for irrigation pumps

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8170.6554Model 10000201210

by Richard Wolf GmbH

Identity

Trade Name
NA FDA UDI
Generic Name
Suction/irrigation tubing, reusable FDA UDI
Device Name
Suction tube set for irrigation pumps EUDAMED
CONNECTION TUBE RECTO PUMP for Recto Pump (connection from device to secretion holder), reusable FDA UDI
Model / Reference
10000201210 EUDAMED
8170.6554 EUDAMED
81706554 FDA UDI
Description
CONNECTION TUBE RECTO PUMP for Recto Pump (connection from device to secretion holder), reusable FDA UDI

Identifiers

Catalog Number
8170.6554 FDA UDI
Primary DI / UDI-DI
04055207057148 EUDAMEDFDA UDI
Basic UDI-DI
405520727052019-0017987QN EUDAMED
Direct Marketing DI
04055207057148 EUDAMED
FDA Product Code
FJL FDA UDI
EMDN Code
A060399 FLUID COLLECTION BAGS AND SYSTEMS - OTHER EUDAMED
GMDN Term
Suction/irrigation tubing, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 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

No

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

Category: General-purpose suction system, pneumatic

Suction tube set for irrigation pumps by Richard Wolf GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, pneumatic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH
EUDAMED SRN
DE-MF-000007048

Sources (2)

  • EUDAMED f1a3f8ed-9d46-4c06-a599-fa139598196a 61 fields · synced Jun 19, 2026
  • FDA UDI 733c3654-e2d0-4c5e-8d80-3e3f9e0f13fb 35 fields · synced May 24, 2026