eudamed_udi
Primary ID: 06430080100224
Suklaa (McLeod) agarmalja (UDI 06430080100224)
Manufactured by Tammer BioLab Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Suklaa (McLeod) agarmalja - Primary ID 06430080100224
Device Regulatory Overview
The Suklaa (McLeod) agarmalja (Model/Catalog Number: T051) is a medical device manufactured by Tammer BioLab Oy. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T051
- Product Code / EMDN
- W0104010405
- Device Name
- Suklaa (McLeod) agarmalja
- Database Sync Date
- 2026-08-09 18:26:34
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 Suklaa (McLeod) agarmalja?
The registered manufacturer of record for Suklaa (McLeod) agarmalja is Tammer BioLab Oy.
What is the Primary UDI-DI identifier for Suklaa (McLeod) agarmalja?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100224.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint