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Aveta Drape Pump 212-081

by Meditrina, Inc.

Aveta Drape Pump 212-081 is a basic roller pump (FDA Class II) made by Meditrina, Inc., listed in FDA GUDID since 11 Apr 2025 (UDI-DI 00850006759811), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850006759811 UDI-DI Date11 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Aveta Drape Pump
Generic name
Basic roller pump
Model / Ref / Catalog
212-081
Primary DI / UDI-DI
00850006759811
FDA product code
HIG, HIH
GMDN term
Basic roller pump
Device class
Class II
Regulation number
884.1700, 884.1690
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HIG (Insufflator, Hysteroscopic).

Other devices from Meditrina, Inc.

See all devices from Meditrina, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)