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03.702.402.97S

by Synthes GmbH

03.702.402.97S (0370240297S) is a Class I device made by Synthes GmbH, listed in FDA GUDID since 31 Dec 2016 (UDI-DI 10886982080615), 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 Number10886982080615 UDI-DI Date31 Dec 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  • Withdrawn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

Generic name
Bone graft delivery kit
Model / Ref / Catalog
03.702.402.97S, 0370240297S
Primary DI / UDI-DI
10886982080615
FDA product code
GEA
GMDN term
Bone graft delivery kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone graft delivery kit

Similar devices

Other devices filed under FDA product code GEA (CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY).

Other devices from Synthes GmbH

  • Tomofix

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  • 68.134.011

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  • Volt 68.134.111

    Class II

See all devices from Synthes GmbH →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)