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MV0613

by Yukon Medical, LLC

MV0613 is a vial/bottle adaptor (FDA Class II; FDA product code LHI, Set, i.V. Fluid transfer) made by Yukon Medical, LLC, listed in FDA GUDID since 7 Jul 2017 (UDI-DI 10885403232671), 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 Number10885403232671 UDI-DI Date7 Jul 2017ListedStatusListed 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  • Withdrawn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

Generic name
Vial/bottle adaptor, non-hermetic
Model / Ref / Catalog
MV0613
Primary DI / UDI-DI
10885403232671
FDA product code
LHI
GMDN term
Vial/bottle adaptor, non-hermetic
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution
Size
Lumen/Inner Diameter — 13 Millimeter

Related devices

Category: Vial/bottle adaptor, non-hermetic

Similar devices in this category

Other devices filed under Vial/bottle adaptor, non-hermetic.

Other devices from Yukon Medical, LLC

See all devices from Yukon Medical, LLC →

Properties

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