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530.660

by Synthes GmbH

530.660 (530660) is a Class I device made by Synthes GmbH, listed in FDA GUDID since 22 May 2017 (UDI-DI 10886982240071), registry data as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10886982240071 UDI-DI Date22 May 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  • Withdrawn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
Surgical power tool battery-exchange sterility cover, reusable
Model / Ref / Catalog
530.660, 530660
Primary DI / UDI-DI
10886982240071
FDA product code
MOQ
GMDN term
Surgical power tool battery-exchange sterility cover, reusable
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical power tool battery-exchange sterility cover

Other devices from Synthes GmbH

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  • 03.111.100S

    Class IIb

  • 68.134.011

    Class II

  • Volt 68.134.111

    Class II

See all devices from Synthes GmbH →

Properties

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