gudid
Primary ID: 9772
Hollister (UDI 9772)
Manufactured by HOLLISTER INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hollister - Primary ID 9772
Device Regulatory Overview
The Hollister (Model/Catalog Number: 9772) is a medical device manufactured by HOLLISTER INCORPORATED. This product is indexed under FDA Product Code / Category Classification GDS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9772
- Product Code / EMDN
- GDS
- Device Name
- Wound Drainage Collector
- Database Sync Date
- 2026-08-09 09:31:01
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 Hollister?
The registered manufacturer of record for Hollister is HOLLISTER INCORPORATED.
What is the Primary UDI-DI identifier for Hollister?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9772.
What classification code is assigned to this device?
This device is registered under product classification code GDS.
Similar Classification Devices (GDS)
Other Devices by HOLLISTER INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint