gudid
Primary ID: RTMTAPE10
Cyotplast RTMTape (UDI RTMTAPE10)
Manufactured by Osteogenics Biomedical Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cyotplast RTMTape - Primary ID RTMTAPE10
Device Regulatory Overview
The Cyotplast RTMTape (Model/Catalog Number: RTMTAPE10) 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
- RTMTAPE10
- Product Code / EMDN
- KGN
- Device Name
- Absorbable Dental Wound Dressing
- Database Sync Date
- 2026-08-09 09:14:58
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 Cyotplast RTMTape?
The registered manufacturer of record for Cyotplast RTMTape is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for Cyotplast RTMTape?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RTMTAPE10.
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
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