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LiquID 071 7F

by Seigla Medical, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850012180036 UDI-DIDate14 Jul 2023ListedStatusListed 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  • Withdrawn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
LiquID 071
Generic Name
Vascular guide-catheter extension
Model / Ref / Catalog
7F, H74939736007 (M2001)
Primary DI / UDI-DI
00850012180036
510(k) Number
FDA Product Code
DQY
GMDN Term
Vascular guide-catheter extension
Device Class
Class II
Regulation Number
870.1250
GUDID distribution status
Not in Commercial Distribution
Size
Catheter Gauge — 7 French

Related devices

Category: Vascular guide-catheter extension

Other devices from Seigla Medical, Inc.

Properties

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

Other properties (9)

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