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Avance Flex 2.0 Negative Pressure Wound Therapy Pump APR100

by Apria Healthcare LLC

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860385000855 UDI-DI Date1 May 2018ListedStatusListed GUDID: not 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  • Withdrawn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
Avance Flex 2.0 Negative Pressure Wound Therapy Pump
Generic Name
Negative-pressure wound therapy system pump, electric
Model / Reference
APR100
Primary DI / UDI-DI
00860385000855
FDA Product Code
OMP
GMDN Term
Negative-pressure wound therapy system pump, electric
Device Class
Class II
Regulation Number
878.4780
GUDID distribution status
Not in Commercial Distribution

Properties

  • Prescription Use
  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No