gudid
Primary ID: GG16010
Ambia (UDI GG16010)
Manufactured by Drgerwerk AG & Co. KGaA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ambia - Primary ID GG16010
Device Regulatory Overview
The Ambia (Model/Catalog Number: GG16010) is a medical device manufactured by Drgerwerk AG & Co. KGaA. This product is indexed under FDA Product Code / Category Classification FQO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GG16010
- Product Code / EMDN
- FQO
- Device Name
- Database Sync Date
- 2026-08-09 09:11:31
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 Ambia?
The registered manufacturer of record for Ambia is Drgerwerk AG & Co. KGaA.
What is the Primary UDI-DI identifier for Ambia?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GG16010.
What classification code is assigned to this device?
This device is registered under product classification code FQO.
Similar Classification Devices (FQO)
Other Devices by Drgerwerk AG & Co. KGaA
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