gudid
Primary ID: 76220
AIMSTEP THYROID SCREEN (UDI 76220)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSTEP THYROID SCREEN - Primary ID 76220
Device Regulatory Overview
The AIMSTEP THYROID SCREEN (Model/Catalog Number: 76220) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification JLW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 76220
- Product Code / EMDN
- JLW
- Device Name
- Cassette test for TSH in fingerstick whole blood
- Database Sync Date
- 2026-08-09 09:04:20
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 AIMSTEP THYROID SCREEN?
The registered manufacturer of record for AIMSTEP THYROID SCREEN is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSTEP THYROID SCREEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 76220.
What classification code is assigned to this device?
This device is registered under product classification code JLW.
Similar Classification Devices (JLW)
Other Devices by GERMAINE LABORATORIES, INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint