gudid
Primary ID: 1.1
RhythmAnalytics (UDI 1.1)
Manufactured by BIOFOURMIS SINGAPORE PTE. LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RhythmAnalytics - Primary ID 1.1
Device Regulatory Overview
The RhythmAnalytics (Model/Catalog Number: 1.1) is a medical device manufactured by BIOFOURMIS SINGAPORE PTE. LTD.. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.1
- Product Code / EMDN
- DQK
- Device Name
- Database Sync Date
- 2026-08-09 09:15:12
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 RhythmAnalytics?
The registered manufacturer of record for RhythmAnalytics is BIOFOURMIS SINGAPORE PTE. LTD..
What is the Primary UDI-DI identifier for RhythmAnalytics?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.1.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by BIOFOURMIS SINGAPORE PTE. LTD.
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