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Dornier MedTech Europe

FDA UDI

Class II (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Dornier MedTech Europe FDA UDI
Generic Name
Urological fluid funnel, sterile FDA UDI
Device Name
Dornier MedTech Europe Urology Drain Bags Vinyl Sterile Fits Dornier Urology Imaging System 20 per Case FDA UDI
Model / Reference
26064 FDA UDI
Description
Dornier MedTech Europe Urology Drain Bags Vinyl Sterile Fits Dornier Urology Imaging System 20 per Case FDA UDI

Identifiers

Catalog Number
26064 FDA UDI
Primary DI / UDI-DI
00618125151967 FDA UDI
FDA Product Code
MMZ FDA UDI
GMDN Term
Urological fluid funnel, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4890 FDA UDI
Commercial Distribution
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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Urological fluid funnel, sterile

Dornier MedTech Europe by Tidi Products, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urological fluid funnel, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI b14ac3ae-172b-4afe-8a36-d535816173d8 34 fields · synced May 30, 2026