← Back to catalogue

Peristeen Plus

FDA UDI

Class II (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Peristeen Plus FDA UDI
Generic Name
Suction/irrigation tubing, reusable FDA UDI
Device Name
Peristeen Plus Transanal Irrigation / Peristeen Plus / Peristeen Plus Transanal irrigation. Tube. 2 tubes with turquoise connectors. FDA UDI
Model / Reference
29146 FDA UDI
Description
Peristeen Plus Transanal Irrigation / Peristeen Plus / Peristeen Plus Transanal irrigation. Tube. 2 tubes with turquoise connectors. FDA UDI

Identifiers

Catalog Number
29146 FDA UDI
Primary DI / UDI-DI
05708932745239 FDA UDI
FDA Product Code
KNT FDA UDI
FCE FDA UDI
GMDN Term
Suction/irrigation tubing, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
876.5210 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suction/irrigation tubing, reusable

Peristeen Plus by Coloplast A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, 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
Coloplast A/S

Sources (1)

  • FDA UDI 71e834cf-28d2-4537-bcd3-ead4a18ecda0 35 fields · synced May 30, 2026