eudamed_udi
Primary ID: B108049POELITEMEU00
BTL-6000 TR-Therapy Elite (UDI B108049POELITEMEU00)
Manufactured by BTL Industries Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BTL-6000 TR-Therapy Elite - Primary ID B108049POELITEMEU00
Device Regulatory Overview
The BTL-6000 TR-Therapy Elite (Model/Catalog Number: P6000.501) is a medical device manufactured by BTL Industries Limited. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P6000.501
- Product Code / EMDN
- Z12069099
- Device Name
- BTL-6000 TR-Therapy
- Database Sync Date
- 2026-08-09 17:11:22
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 BTL-6000 TR-Therapy Elite?
The registered manufacturer of record for BTL-6000 TR-Therapy Elite is BTL Industries Limited.
What is the Primary UDI-DI identifier for BTL-6000 TR-Therapy Elite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B108049POELITEMEU00.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by BTL Industries Limited
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