BOND (UDI BOND Universal Covertiles (pack of 160))
Manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD
Device Regulatory Overview
The BOND (Model/Catalog Number: BOND Universal Covertiles (pack of 160)) is a medical device manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD. This product is indexed under FDA Product Code / Category Classification KPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BOND Universal Covertiles (pack of 160)
- Product Code / EMDN
- KPA
- Device Name
- Transparent plastic covers that sit over slides during staining, provided in a pack of 160.
- Database Sync Date
- 2026-08-09 09:38:27
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 BOND?
The registered manufacturer of record for BOND is LEICA BIOSYSTEMS MELBOURNE PTY LTD.
What is the Primary UDI-DI identifier for BOND?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BOND Universal Covertiles (pack of 160).
What classification code is assigned to this device?
This device is registered under product classification code KPA.
Similar Classification Devices (KPA)
Other Devices by LEICA BIOSYSTEMS MELBOURNE PTY LTD
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