gudid
Primary ID: LUBRICATING GEL
AQUAGEL (UDI LUBRICATING GEL)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AQUAGEL - Primary ID LUBRICATING GEL
Device Regulatory Overview
The AQUAGEL (Model/Catalog Number: LUBRICATING GEL) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification KMJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LUBRICATING GEL
- Product Code / EMDN
- KMJ
- Device Name
- AQUAGEL LUBRICATING GEL 20 g packette
- Database Sync Date
- 2026-08-09 09:49:29
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 AQUAGEL?
The registered manufacturer of record for AQUAGEL is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for AQUAGEL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LUBRICATING GEL.
What classification code is assigned to this device?
This device is registered under product classification code KMJ.
Similar Classification Devices (KMJ)
Other Devices by PARKER LABORATORIES INC
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