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BandNet® 5011

by Derma Sciences Canada, Inc

BandNet® 5011 (BA5011) is a Class I device made by Derma Sciences Canada, Inc, listed in FDA GUDID since 23 Oct 2018 (UDI-DI 00809958001790), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00809958001790 UDI-DI Date23 Oct 2018ListedStatusListed 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  • Withdrawn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
BandNet®
Generic name
Stockinette
Model / Ref / Catalog
5011, BA5011
Primary DI / UDI-DI
00809958001790
FDA product code
FQM
GMDN term
Stockinette
Device class
Class I
Regulation number
880.5075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Stockinette

Similar devices in this category

Other devices filed under Stockinette.

Other devices from DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.)

See all devices from DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.) →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)