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Vesco Medical 12FR 91cm Adult (PU) Dual ENFit Port NG Tube VED-29112

by Vesco Medical LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810096150011 UDI-DI Date2 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Vesco Medical 12FR 91cm Adult (PU) Dual ENFit Port NG Tube
Generic Name
Nasogastric feeding tube
Model / Reference
VED-29112
Primary DI / UDI-DI
00810096150011
510(k) Number
FDA Product Code
PIF
GMDN Term
Nasogastric feeding tube
Device Class
Class II
Regulation Number
876.5980
GUDID distribution status
In Commercial Distribution
Size
Length — 91 Centimeter
Catheter Gauge — 12 French

Related devices

Cleared under the same submission (K170162)

Show all (12)

Other devices from Vesco Medical LLC

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Properties

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

Other properties (10)

  • Sterile: No
  • 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