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Arthrex® AR-3490-02

by Arthrex, Inc. United States GUDID

Product code NBH

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888867030954 UDI-DIDate20 Jun 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
Arthrex®
Generic Name
Arthroscopic sleeve-seal connector
Model / Ref / Catalog
AR-3490-02
Primary DI / UDI-DI
00888867030954
FDA Product Code
NBH
GMDN Term
Arthroscopic sleeve-seal connector
Device Class
Class I
Regulation Number
888.1100
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date
Other properties (10)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No

Sources (1)

  • FDA UDI d8e9fae8-bb16-4040-8f04-de6abaeee1d6 35 fields · synced 23 Oct 2026