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Timm

FDA UDI

Class II (US FDA UDI)

by Mediplus , Ltd.

Identity

Trade Name
TIMM FDA UDI
Generic Name
Urological irrigation system FDA UDI
Device Name
Long water tubing kit FDA UDI
Model / Reference
TIMM84411226-2 FDA UDI
Description
Long water tubing kit FDA UDI

Identifiers

Primary DI / UDI-DI
05055140703422 FDA UDI
FDA Product Code
FEN FDA UDI
GMDN Term
Urological irrigation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1620 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Timm by Mediplus , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mediplus , Ltd.

Sources (1)

  • FDA UDI 4dd2a8c0-1089-4a27-a8ee-0213050747aa 35 fields · synced Jun 8, 2026