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GoBack Crossing Catheter GB 603-US 014P 80L

by Upstream Peripheral Technologies GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290017837239 UDI-DIDate19 Oct 2022ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
GoBack Crossing Catheter
Generic Name
Peripheral vascular intervention infusion catheter
Model / Reference
GB 603-US 014P 80L
Primary DI / UDI-DI
07290017837239
FDA Product Code
PDU
GMDN Term
Peripheral vascular intervention infusion catheter
Device Class
Class II
Regulation Number
870.1250
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from Upstream Peripheral Technologies

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Manufacturing Date: No