gudid
Primary ID: 712M08-G
Generic (UDI 712M08-G)
Manufactured by CHEMTRON BIOTECH INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Generic - Primary ID 712M08-G
Device Regulatory Overview
The Generic (Model/Catalog Number: 712M08-G) is a medical device manufactured by CHEMTRON BIOTECH INC. This product is indexed under FDA Product Code / Category Classification LAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 712M08-G
- Product Code / EMDN
- LAF
- Device Name
- 13-Panel DOA Cup, AMP500/BAR/BUP/BZO/COC150/FYL5/MDMA/MET/MTD/MOR/OXY/PCP/THC, 25tests/kit
- Database Sync Date
- 2026-08-09 09:22:09
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 Generic?
The registered manufacturer of record for Generic is CHEMTRON BIOTECH INC.
What is the Primary UDI-DI identifier for Generic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 712M08-G.
What classification code is assigned to this device?
This device is registered under product classification code LAF.
Similar Classification Devices (LAF)
Other Devices by CHEMTRON BIOTECH INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint