gudid
Primary ID: 1
Emdogain (UDI 1)
Manufactured by Institut Straumann AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Emdogain - Primary ID 1
Device Regulatory Overview
The Emdogain (Model/Catalog Number: 1) is a medical device manufactured by Institut Straumann AG. This product is indexed under FDA Product Code / Category Classification NQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- NQA
- Device Name
- Straumann Emdogain 0.15 ml, Enamel Matrix Derivative 30 mg/ml, contains 5 syringes Straumann Emdogain 0.15 ml and 5 blunt needles
- Database Sync Date
- 2026-08-09 09:19:47
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 Emdogain?
The registered manufacturer of record for Emdogain is Institut Straumann AG.
What is the Primary UDI-DI identifier for Emdogain?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code NQA.
Similar Classification Devices (NQA)
Other Devices by Institut Straumann AG
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