gudid
Primary ID: 4010-U-P
Rescuer BVM Manual Resuscitator (UDI 4010-U-P)
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 Rescuer BVM Manual Resuscitator - Primary ID 4010-U-P
Device Regulatory Overview
The Rescuer BVM Manual Resuscitator (Model/Catalog Number: 4010-U-P) 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
- 4010-U-P
- Product Code / EMDN
- BTM
- Device Name
- Rescuer branded child disposable BVM Manual Resuscitator with 2900 mL reservoir, #3 cushion mask, 2 mL crush proof oxygen tubing (universal connector) and attached 0-20 cmH2O PEEP valve
- Database Sync Date
- 2026-08-09 09:16:44
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 Rescuer BVM Manual Resuscitator?
The registered manufacturer of record for Rescuer BVM Manual Resuscitator is B.L.S. Systems Limited.
What is the Primary UDI-DI identifier for Rescuer BVM Manual Resuscitator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4010-U-P.
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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