gudid
Primary ID: RTMPLUG10
Cytoplast RTMPlug (UDI RTMPLUG10)
Manufactured by Osteogenics Biomedical Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cytoplast RTMPlug - Primary ID RTMPLUG10
Device Regulatory Overview
The Cytoplast RTMPlug (Model/Catalog Number: RTMPLUG10) is a medical device manufactured by Osteogenics Biomedical Inc. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RTMPLUG10
- Product Code / EMDN
- KGN
- Device Name
- Absorbable Dental Wound Dressing
- Database Sync Date
- 2026-08-09 09:14:58
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 Cytoplast RTMPlug?
The registered manufacturer of record for Cytoplast RTMPlug is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for Cytoplast RTMPlug?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RTMPLUG10.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by Osteogenics Biomedical Inc
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint