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Velnez 140402

by Datt Mediproducts Private Limited

Velnez 140402 is a Class I device made by Datt Mediproducts Private Limited, listed in FDA GUDID since 21 Jun 2023 (UDI-DI 08904340407616), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08904340407616 UDI-DI Date21 Jun 2023ListedStatusListed 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  • Withdrawn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
Velnez
Generic name
Intranasal splint, non-bioabsorbable, animal-derived
Model / reference
140402
Primary DI / UDI-DI
08904340407616
FDA product code
LYA
GMDN term
Intranasal splint, non-bioabsorbable, animal-derived
Device class
Class I
Regulation number
874.4780
GUDID distribution status
In Commercial Distribution
Size
Length — 4 Centimeter
Width — 2 Centimeter

Similar devices

Other devices filed under FDA product code LYA (Splint, Intranasal Septal).

Other devices from Datt Mediproducts Private Limited

See all devices from Datt Mediproducts Private Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)