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Restrata(R) RWM1-2.5X7

by Acera Surgical Inc

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854258006389 UDI-DI Date15 Apr 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  • Withdrawn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
Restrata(R)
Generic Name
Synthetic wound matrix dressing
Model / Reference
RWM1-2.5X7
Primary DI / UDI-DI
00854258006389
FDA Product Code
QSZ
GMDN Term
Synthetic wound matrix dressing
Device Class
U
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Length — 5.0 Centimeter
Width — 2.5 Centimeter

Other devices from Acera Surgical Inc

See all devices from Acera Surgical Inc →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration 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
  • Manufacturing Date: No