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Na Cb-1.A

by S & T AG United States GUDID

Product code FSM

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberESOT010801 UDI-DIDate20 Jan 2026ListedStatusIn 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
Na
Generic Name
Surgical instrument/implant rack
Model / Ref / Catalog
CB-1.A, 01080
Primary DI / UDI-DI
ESOT010801
FDA Product Code
FSM
GMDN Term
Surgical instrument/implant rack
Device Class
Class I
Regulation Number
878.4800
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from S & T AG

See all devices from S & T AG →

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 d4194113-e287-4c94-abe1-3776a51eab4e 35 fields · synced 23 Oct 2026