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Eclipse 1500-02-000

by Medshape, Inc.

Eclipse 1500-02-000 is a Class I device made by Medshape, Inc., listed in FDA GUDID since 19 May 2017 (UDI-DI M9701500020000), 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 NumberM9701500020000 UDI-DI Date19 May 2017ListedStatusListed 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  • Withdrawn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
Eclipse
Generic name
Suturing unit, single-use
Model / reference
1500-02-000
Primary DI / UDI-DI
M9701500020000
FDA product code
KDD
GMDN term
Suturing unit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bone pin, non-bioabsorbableSuturing unit, single-useLigament graft sizer, noninvasiveSuture knot pusher, single-use

Similar devices

Other devices filed under FDA product code KDD (Kit, Surgical Instrument, Disposable).

Other devices from Medshape, Inc.

See all devices from Medshape, Inc. →

Properties

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