SS Agar Plate (Salmonella Shigella Agar) (UDI 08606018770038)
Manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA
Device Regulatory Overview
The SS Agar Plate (Salmonella Shigella Agar) (Model/Catalog Number: PRM1032V20) is a medical device manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRM1032V20
- Product Code / EMDN
- W0104010405
- Device Name
- SS Agar Plate (Salmonella Shigella Agar)
- Database Sync Date
- 2026-08-09 16:30:18
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 SS Agar Plate (Salmonella Shigella Agar)?
The registered manufacturer of record for SS Agar Plate (Salmonella Shigella Agar) is DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA.
What is the Primary UDI-DI identifier for SS Agar Plate (Salmonella Shigella Agar)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08606018770038.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
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