OstomyGel (UDI 290010003)
Manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
Device Regulatory Overview
The OstomyGel (Model/Catalog Number: 290010003) is a medical device manufactured by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA. This product is indexed under FDA Product Code / Category Classification GDS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 290010003
- Product Code / EMDN
- GDS
- Device Name
- Ostomy accessory
- Database Sync Date
- 2026-08-09 09:07:18
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 OstomyGel?
The registered manufacturer of record for OstomyGel is DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA.
What is the Primary UDI-DI identifier for OstomyGel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 290010003.
What classification code is assigned to this device?
This device is registered under product classification code GDS.
Similar Classification Devices (GDS)
Other Devices by DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA
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