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Peristeen

FDA UDI

Class II (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Peristeen FDA UDI
Generic Name
Rectal irrigation system catheter FDA UDI
Device Name
Peristeen Transanal Irrigation. Accessory unit. 15 rectal catheters Small, 1 water bag. Non sterile. Rx only. FDA UDI
Model / Reference
29127 FDA UDI
Description
Peristeen Transanal Irrigation. Accessory unit. 15 rectal catheters Small, 1 water bag. Non sterile. Rx only. FDA UDI

Identifiers

Catalog Number
29127 FDA UDI
Primary DI / UDI-DI
05708932514934 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Rectal irrigation system catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

Yes

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: Rectal irrigation system catheterRectal irrigation system fluid container

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

Similar devices

Also classified as Rectal irrigation system fluid container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI 1c03d491-376b-41d2-9004-35756c5a99e3 37 fields · synced May 30, 2026