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Aesculap JF126R

by Aesculap, Inc. United States GUDID

Product code FSM

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046955775002 UDI-DIDate31 Oct 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

GUDID · synced 22 Oct 2026

Trade Name
Aesculap
Generic Name
Surgical instrument/implant rack
Model / Ref / Catalog
JF126R
Primary DI / UDI-DI
04046955775002
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 Aesculap, Inc.

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Properties & raw data

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

Sources (1)

  • FDA UDI 5a64f885-8a5c-4608-b684-102b55d00be4 35 fields · synced 22 Oct 2026