gudid
Primary ID: 6690-1A
6690 (UDI 6690-1A)
Manufactured by TUTTNAUER ISRAEL LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 6690 - Primary ID 6690-1A
Device Regulatory Overview
The 6690 (Model/Catalog Number: 6690-1A) is a medical device manufactured by TUTTNAUER ISRAEL LTD.. This product is indexed under FDA Product Code / Category Classification FLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6690-1A
- Product Code / EMDN
- FLE
- Device Name
- Sterilizer,steam
- Database Sync Date
- 2026-08-09 09:18:12
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 6690?
The registered manufacturer of record for 6690 is TUTTNAUER ISRAEL LTD..
What is the Primary UDI-DI identifier for 6690?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6690-1A.
What classification code is assigned to this device?
This device is registered under product classification code FLE.
Similar Classification Devices (FLE)
Other Devices by TUTTNAUER ISRAEL LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint