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Brava 032205

by Coloplast A/S

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 Number05708932702638 UDI-DI Date8 Apr 2022ListedStatusListed 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  • Withdrawn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
Brava
Generic Name
Pressure bandage, non-latex, single-use
Model / Ref / Catalog
032205
Description
Brava Protective Sheet / Brava Ostomy bag / Brava / Coloplast Protective Sheet. Ostomy Care.
Primary DI / UDI-DI
05708932702638
FDA Product Code
NAD
GMDN Term
Pressure bandage, non-latex, single-use
Device Class
Class I
Regulation Number
878.4020
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Length — 8 Inch
Width — 20 Centimeter
Width — 8 Inch
Length — 20 Centimeter

Related devices

Category: Pressure bandage, non-latex, single-use

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No