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Reli SN26G351

by Myco Medical Supplies Inc.

Reli SN26G351 is a Class II device made by Myco Medical Supplies Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00386120006970), 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 Number00386120006970 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Reli
Generic name
Spinal needle, single-use
Model / reference
SN26G351
Primary DI / UDI-DI
00386120006970
FDA product code
BSP
GMDN term
Spinal needle, single-use
Device class
Class II
Regulation number
868.5150
GUDID distribution status
In Commercial Distribution
Size
Length — 3.5 Inch
Needle Gauge — 26 Gauge

Similar devices

Other devices filed under FDA product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)).

Other devices from Myco Medical Supplies Inc.

See all devices from Myco Medical Supplies Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)