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eXact 5.1 CM3051

by Cypris Medical

eXact 5.1 CM3051 is a Class I device made by Cypris Medical, listed in FDA GUDID since 28 Feb 2023 (UDI-DI 00854037007149), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854037007149 UDI-DI Date28 Feb 2023ListedStatusListed 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  • Withdrawn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
eXact 5.1
Generic name
Suturing unit, single-use
Model / reference
CM3051
Primary DI / UDI-DI
00854037007149
FDA product code
GEJ
GMDN term
Suturing unit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suturing unit, single-use

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Other devices filed under Suturing unit, single-use.

Other devices from Cypris Medical

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)