gudid
Primary ID: PL.160R
Microbank Red (80 vials) (UDI PL.160R)
Manufactured by PRO-LAB, INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Microbank Red (80 vials) - Primary ID PL.160R
Device Regulatory Overview
The Microbank Red (80 vials) (Model/Catalog Number: PL.160R) is a medical device manufactured by PRO-LAB, INCORPORATED. This product is indexed under FDA Product Code / Category Classification JSC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PL.160R
- Product Code / EMDN
- JSC
- Device Name
- Single vials of Microbank
- Database Sync Date
- 2026-08-09 09:37:15
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 Microbank Red (80 vials)?
The registered manufacturer of record for Microbank Red (80 vials) is PRO-LAB, INCORPORATED.
What is the Primary UDI-DI identifier for Microbank Red (80 vials)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PL.160R.
What classification code is assigned to this device?
This device is registered under product classification code JSC.
Similar Classification Devices (JSC)
Other Devices by PRO-LAB, INCORPORATED
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