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VWING Vascular Needle Guide 00149

by Vital Access United States GUDID

Product code PFH

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08199260101496 UDI-DIDate4 Feb 2015ListedStatusIn 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
VWING Vascular Needle Guide
Generic Name
Arteriovenous fistula buttonhole cannulation guide
Model / Ref / Catalog
00149
Primary DI / UDI-DI
08199260101496
FDA Product Code
PFH
GMDN Term
Arteriovenous fistula buttonhole cannulation guide
Device Class
Class II
Regulation Number
876.5540
Commercial Distribution
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 18 Millimeter
Width — 9 Millimeter
Height — 10 Millimeter

Other devices from Vital Access

See all devices from Vital Access →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
Other properties (8)
  • 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

Sources (1)

  • FDA UDI 96788257-b5ab-4eff-8996-b7ecc211763c 37 fields · synced 23 Oct 2026