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Crimper 9100CR23

by Edwards Lifesciences LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00690103177985 UDI-DI Date30 Aug 2014ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Crimper
Generic name
Basic crimper
Model / Ref / Catalog
9100CR23
Primary DI / UDI-DI
00690103177985
FDA product code
NPT
GMDN term
Basic crimper
Device class
Class III
GUDID distribution status
In Commercial Distribution

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Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (5)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Premarket exempt: No
  • Serial number: No