gudid
Primary ID: 157100100
RUSCH (UDI 157100100)
Manufactured by B.L.S. Systems Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RUSCH - Primary ID 157100100
Device Regulatory Overview
The RUSCH (Model/Catalog Number: 157100100) is a medical device manufactured by B.L.S. Systems Limited. This product is indexed under FDA Product Code / Category Classification BTM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 157100100
- Product Code / EMDN
- BTM
- Device Name
- Blue RUSCH branded adult manual resuscitator, oxygen reservoir tubing, swivel connector, medication port, Peep connector and medium mask
- Database Sync Date
- 2026-08-09 09:50:05
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 B.L.S. Systems Limited.
What is the Primary UDI-DI identifier for RUSCH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 157100100.
What classification code is assigned to this device?
This device is registered under product classification code BTM.
Similar Classification Devices (BTM)
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