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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
Rolling stand for 1 or 2 pumps FDA UDI
Model / Reference
211402 FDA UDI
Description
Rolling stand for 1 or 2 pumps FDA UDI

Identifiers

Catalog Number
S079021D FDA UDI
Primary DI / UDI-DI
04260123933982 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 75377423-88db-4d17-be34-88cedef67590 34 fields · synced Jun 8, 2026