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Mixor 71270042

by Smith & Nephew, Inc.

Mixor 71270042 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 29 Aug 2015 (UDI-DI 03596010384607), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03596010384607 UDI-DI Date29 Aug 2015ListedStatusListed 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  • Withdrawn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
Mixor
Generic name
Noninvasive manual orthopaedic cement preparation kit, reusable
Model / Ref / Catalog
71270042
Primary DI / UDI-DI
03596010384607
FDA product code
JDZ
GMDN term
Noninvasive manual orthopaedic cement preparation kit, reusable
Device class
Class I
Regulation number
888.4210
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Manual orthopaedic cement mixer, reusable

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Other devices filed under Manual orthopaedic cement mixer, reusable.

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Properties

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