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Spinr™ 00884450277225

by Merit Medical Systems, Inc.

Spinr™ 00884450277225 is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00884450277225), 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 Number00884450277225 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  • Withdrawn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
Spinr™
Generic name
Torque manipulation device
Model / reference
00884450277225
Primary DI / UDI-DI
00884450277225
FDA product code
DQX
GMDN term
Torque manipulation device
Device class
Class II
Regulation number
870.1330
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DQX (WIRE, GUIDE, CATHETER).

Other devices from Merit Medical Systems, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)