gudid
Primary ID: 221500160
RUSCH (UDI 221500160)
Manufactured by TELEFLEX INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RUSCH - Primary ID 221500160
Device Regulatory Overview
The RUSCH (Model/Catalog Number: 221500160) is a medical device manufactured by TELEFLEX INCORPORATED. This product is indexed under FDA Product Code / Category Classification GBM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 221500160
- Product Code / EMDN
- GBM
- Device Name
- Database Sync Date
- 2026-08-09 09:00:28
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 RUSCH?
The registered manufacturer of record for RUSCH is TELEFLEX INCORPORATED.
What is the Primary UDI-DI identifier for RUSCH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 221500160.
What classification code is assigned to this device?
This device is registered under product classification code GBM.
Similar Classification Devices (GBM)
Other Devices by TELEFLEX INCORPORATED
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