gudid
Primary ID: 21300650
Perfectim 90 Second Flexi-Velvet (UDI 21300650)
Manufactured by J. MORITA U.S.A., INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perfectim 90 Second Flexi-Velvet - Primary ID 21300650
Device Regulatory Overview
The Perfectim 90 Second Flexi-Velvet (Model/Catalog Number: 21300650) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21300650
- Product Code / EMDN
- ELW
- Device Name
- PVS Dental Impression Material
- Database Sync Date
- 2026-08-09 09:58:58
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 Perfectim 90 Second Flexi-Velvet?
The registered manufacturer of record for Perfectim 90 Second Flexi-Velvet is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for Perfectim 90 Second Flexi-Velvet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21300650.
What classification code is assigned to this device?
This device is registered under product classification code ELW.
Similar Classification Devices (ELW)
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