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V.A.T.S. Mayo Hegar Needle Holder 2300-9041

by Sontec Instruments, Inc. 2 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB099230090410 UDI-DI Date16 May 2018ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
V.A.T.S. Mayo Hegar Needle Holder
Generic Name
Suturing needle holder, reusable
Model / Reference
2300-9041
Primary DI / UDI-DI
B099230090410
510(k) Number
FDA Product Code
GCJ
GMDN Term
Suturing needle holder, reusable
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
Not in Commercial Distribution
Size
Length — 13 Inch

Other devices from Sontec Instruments, Inc.

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No