Mueller Hinton Agar Plate No. 2 (UDI 08606018770809)
Manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA
Device Regulatory Overview
The Mueller Hinton Agar Plate No. 2 (Model/Catalog Number: PRM1084V60) is a medical device manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRM1084V60
- Product Code / EMDN
- W0104010403
- Device Name
- Mueller Hinton Agar Plate No. 2
- Database Sync Date
- 2026-08-09 18:58:38
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 Mueller Hinton Agar Plate No. 2?
The registered manufacturer of record for Mueller Hinton Agar Plate No. 2 is DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA.
What is the Primary UDI-DI identifier for Mueller Hinton Agar Plate No. 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08606018770809.
What classification code is assigned to this device?
This device is registered under product classification code W0104010403.
Similar Classification Devices (W0104010403)
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