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Anovo MULTI-PORT STERILE DRAPE FP-04-0020

by Pharma Sept Medical Products (1995) Ltd.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00836230005092 UDI-DI Date15 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Anovo MULTI-PORT STERILE DRAPE
Generic Name
Medical equipment/instrument drape, single-use
Model / Reference
FP-04-0020
Primary DI / UDI-DI
00836230005092
FDA Product Code
QNM
GMDN Term
Medical equipment/instrument drape, single-use
Device Class
Class II
Regulation Number
878.4961
GUDID distribution status
In Commercial Distribution

Other devices from Pharma Sept Medical Products (1995) Ltd.

See all devices from Pharma Sept Medical Products (1995) Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No