gudid
Primary ID: 21300700
Perfectim Single Phase Body (UDI 21300700)
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 Single Phase Body - Primary ID 21300700
Device Regulatory Overview
The Perfectim Single Phase Body (Model/Catalog Number: 21300700) 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
- 21300700
- Product Code / EMDN
- ELW
- Device Name
- PVS Dental Impression Material
- Database Sync Date
- 2026-08-09 09:58:58
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Perfectim Single Phase Body?
The registered manufacturer of record for Perfectim Single Phase Body is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for Perfectim Single Phase Body?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21300700.
What classification code is assigned to this device?
This device is registered under product classification code ELW.
Similar Classification Devices (ELW)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint