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Provita

FDA UDI

Class I (US FDA UDI)

by provita medical gmbh & co. kg

Identity

Trade Name
Provita FDA UDI
Generic Name
Transportable medical equipment stand, non-powered FDA UDI
Device Name
MULTICHANNEL ROLLING STAND FDA UDI
Model / Reference
211396 FDA UDI
Description
MULTICHANNEL ROLLING STAND FDA UDI

Identifiers

Catalog Number
S079011D FDA UDI
Primary DI / UDI-DI
04260123933975 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Transportable medical equipment stand, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Freestanding/bed-attached intravenous poleTransportable medical equipment stand, non-powered

Provita by provita medical gmbh & co. kg — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transportable medical equipment stand, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
provita medical gmbh & co. kg

Sources (1)

  • FDA UDI b0c4f8cb-23a6-4584-b181-645a822ae538 34 fields · synced May 30, 2026