VaPro Pocket 77144

by Hollister Incorporated GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number20610075090789 UDI-DI	Date1 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: VaPro Pocket
Generic Name: Single-administration urethral drainage catheter
Model / Reference: 77144

Primary DI / UDI-DI: 20610075090789
510(k) Number: K143594
FDA Product Code: GBM
GMDN Term: Single-administration urethral drainage catheter

Device Class: Class II
Regulation Number: 876.5130
GUDID distribution status: In Commercial Distribution

Size: Catheter Gauge — 14 French
Length — 16 Inch

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Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number
Expiration Date
Manufacturing 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
Serial Number: No