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Aveta Drape Pump

FDA UDI

Class II (US FDA UDI)

by Meditrina, Inc.

Identity

Trade Name
Aveta Drape Pump FDA UDI
Generic Name
Basic roller pump FDA UDI
Device Name
Aveta Drape Pump FDA UDI
Model / Reference
212-081 FDA UDI
Description
Aveta Drape Pump FDA UDI

Identifiers

Catalog Number
212-081 FDA UDI
Primary DI / UDI-DI
00850006759811 FDA UDI
FDA Product Code
HIG FDA UDI
HIH FDA UDI
GMDN Term
Basic roller pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1700 FDA UDI
884.1690 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic roller pump

Aveta Drape Pump by Meditrina, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic roller pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meditrina, Inc.

Sources (1)

  • FDA UDI f4bf4abb-83e6-432d-96a5-e58be27bd6f5 34 fields · synced May 30, 2026