gudid
Primary ID: 9775
Hollister (UDI 9775)
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 9775
Device Regulatory Overview
The Hollister (Model/Catalog Number: 9775) 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
- 9775
- Product Code / EMDN
- GDS
- Device Name
- Wound Drainage Collector
- Database Sync Date
- 2026-08-09 09:31:01
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 9775.
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
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