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ECHOBRIGHT* ECHOGENIC Regional Block Needle with Injection Set 120008740

by Avanos Medical, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00193494001780 UDI-DI Date28 Nov 2025ListedStatusListed 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  • Withdrawn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
ECHOBRIGHT* ECHOGENIC Regional Block Needle with Injection Set
Generic Name
Peripheral anaesthesia single-administration set, non-medicated
Model / Ref / Catalog
120008740, EBL20100SG
Primary DI / UDI-DI
00193494001780
FDA Product Code
BSP
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated
Device Class
Class II
Regulation Number
868.5150
GUDID distribution status
In Commercial Distribution

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See all devices from Avanos Medical, Inc. →

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