DLK900 DataLINK - Plastic connectors (UDI 05060481691925)
Manufactured by Biometrics Ltd
Device Regulatory Overview
The DLK900 DataLINK - Plastic connectors (Model/Catalog Number: DLK900 DataLINK) is a medical device manufactured by Biometrics Ltd. This product is indexed under FDA Product Code / Category Classification Z120605,Z120617 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DLK900 DataLINK
- Product Code / EMDN
- Z120605,Z120617
- Device Name
- Data Acquisition Products
- Database Sync Date
- 2026-08-09 18:34:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DLK900 DataLINK - Plastic connectors?
The registered manufacturer of record for DLK900 DataLINK - Plastic connectors is Biometrics Ltd.
What is the Primary UDI-DI identifier for DLK900 DataLINK - Plastic connectors?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060481691925.
What classification code is assigned to this device?
This device is registered under product classification code Z120605,Z120617.
Similar Classification Devices (Z120605,Z120617)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint