gudid
Primary ID: 09120052070514
PROFI BLOT T48 (UDI 09120052070514)
Manufactured by Tecan Austria GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROFI BLOT T48 - Primary ID 09120052070514
Device Regulatory Overview
The PROFI BLOT T48 (Model/Catalog Number: 09120052070514) is a medical device manufactured by Tecan Austria GmbH. This product is indexed under FDA Product Code / Category Classification KPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09120052070514
- Product Code / EMDN
- KPA
- Device Name
- Database Sync Date
- 2026-08-09 09:29:32
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 PROFI BLOT T48?
The registered manufacturer of record for PROFI BLOT T48 is Tecan Austria GmbH.
What is the Primary UDI-DI identifier for PROFI BLOT T48?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09120052070514.
What classification code is assigned to this device?
This device is registered under product classification code KPA.
Similar Classification Devices (KPA)
Other Devices by Tecan Austria GmbH
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