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Reli Btd-Ml

by Myco Medical Supplies Inc.

Reli Btd-Ml is a Class I device made by Myco Medical Supplies Inc., listed in FDA GUDID since 7 Jun 2023 (UDI-DI 00386120012193), 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 Number00386120012193 UDI-DI Date7 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  • Withdrawn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
Reli
Generic name
Blood collection tube holder/needle
Model / Ref / Catalog
BTD-ML
Primary DI / UDI-DI
00386120012193
FDA product code
KST
GMDN term
Blood collection tube holder/needle
Device class
Class I
Regulation number
864.9125
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood collection tube holder/needle

Other devices from Myco Medical Supplies Inc.

See all devices from Myco Medical Supplies Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)