LDH SL R1:6x20ml,R2:2x15ml(HIT) (UDI 05213003191506)
Manufactured by Biotechnological Applications Ltd
Device Regulatory Overview
The LDH SL R1:6x20ml,R2:2x15ml(HIT) (Model/Catalog Number: 001520) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010120 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 001520
- Product Code / EMDN
- W01010120
- Device Name
- LDH SL R1:6x20ml,R2:2x15ml(HIT)
- Database Sync Date
- 2026-08-09 16:50:09
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 LDH SL R1:6x20ml,R2:2x15ml(HIT)?
The registered manufacturer of record for LDH SL R1:6x20ml,R2:2x15ml(HIT) is Biotechnological Applications Ltd.
What is the Primary UDI-DI identifier for LDH SL R1:6x20ml,R2:2x15ml(HIT)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003191506.
What classification code is assigned to this device?
This device is registered under product classification code W01010120.
Similar Classification Devices (W01010120)
Other Devices by Biotechnological Applications Ltd
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