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Cushing Brain Depressor 412-789

by Sontec Instruments, Inc. United States GUDID

Product code GAF

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896036277 UDI-DIDate13 Sep 2018ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Cushing Brain Depressor
Generic Name
Vessel depressor
Model / Ref / Catalog
412-789
Primary DI / UDI-DI
00192896036277
FDA Product Code
GAF
GMDN Term
Vessel depressor
Device Class
Class I
Regulation Number
878.4800
Commercial Distribution
In Commercial Distribution
Size
Length — 7.75 Inch

Related devices

Category: Vessel depressor

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
Other properties (11)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI e15e9d2a-2214-423e-8654-8bf7b3b64bb6 36 fields · synced 23 Oct 2026