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Navina™ Tube Set

FDA UDI

Class II (US FDA UDI)

by Wellspect AB

Identity

Trade Name
Navina™ Tube Set FDA UDI
Generic Name
Rectal irrigation kit FDA UDI
Device Name
Navina Transanal Irrigation. Tube set. 1 Water container tube, 1 Rectal catheter tube. Non Sterile Device. Rx Only. FDA UDI
Model / Reference
69011 FDA UDI
Description
Navina Transanal Irrigation. Tube set. 1 Water container tube, 1 Rectal catheter tube. Non Sterile Device. Rx Only. FDA UDI

Identifiers

Catalog Number
6901140 FDA UDI
Primary DI / UDI-DI
07333387027999 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Rectal irrigation kit 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

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: Rectal irrigation kit

Navina™ Tube Set by Wellspect AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rectal irrigation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wellspect AB

Sources (1)

  • FDA UDI 396e2d37-36cf-4714-a350-17e8f79fb5d1 35 fields · synced Jun 6, 2026