GUDIDData
gudid Primary ID: 70164

VaPro Pocket (UDI 70164)

Manufactured by HOLLISTER INCORPORATED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VaPro Pocket - Primary ID 70164

Device Regulatory Overview

The VaPro Pocket (Model/Catalog Number: 70164) is a medical device manufactured by HOLLISTER INCORPORATED. This product is indexed under FDA Product Code / Category Classification GBM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
70164
Product Code / EMDN
GBM
Device Name
No Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve
Database Sync Date
2026-08-09 09:22:50

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of VaPro Pocket?

The registered manufacturer of record for VaPro Pocket is HOLLISTER INCORPORATED.

What is the Primary UDI-DI identifier for VaPro Pocket?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 70164.

What classification code is assigned to this device?

This device is registered under product classification code GBM.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint