gudid
Primary ID: BIT23A
BICEL I/A curved / 23G terralution (UDI BIT23A)
Manufactured by Medicel AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BICEL I/A curved / 23G terralution - Primary ID BIT23A
Device Regulatory Overview
The BICEL I/A curved / 23G terralution (Model/Catalog Number: BIT23A) is a medical device manufactured by Medicel AG. This product is indexed under FDA Product Code / Category Classification HMX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BIT23A
- Product Code / EMDN
- HMX
- Device Name
- I/A handpiece
- Database Sync Date
- 2026-08-09 09:03:20
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 BICEL I/A curved / 23G terralution?
The registered manufacturer of record for BICEL I/A curved / 23G terralution is Medicel AG.
What is the Primary UDI-DI identifier for BICEL I/A curved / 23G terralution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BIT23A.
What classification code is assigned to this device?
This device is registered under product classification code HMX.
Similar Classification Devices (HMX)
Other Devices by Medicel AG
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