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Phoenix INT201250

by Dr.japan Co., Ltd.

Phoenix INT201250 is a Class II device made by Dr.japan Co., Ltd., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 44900719911021), 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 Number44900719911021 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  • Withdrawn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
Phoenix
Generic name
Spinal needle, single-use
Model / reference
INT201250
Primary DI / UDI-DI
44900719911021
FDA product code
BSP
GMDN term
Spinal needle, single-use
Device class
Class II
Regulation number
868.5150
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Length — 30 Millimeter
Needle Gauge — 20 Gauge

Related devices

Category: Spinal needle, single-use

Similar devices

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

Other devices from Dr.japan Co., Ltd.

See all devices from Dr.japan Co., Ltd. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)