gudid
Primary ID: ZD1520TK
ZDERM (UDI ZD1520TK)
Manufactured by Osteogenics Biomedical Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZDERM - Primary ID ZD1520TK
Device Regulatory Overview
The ZDERM (Model/Catalog Number: ZD1520TK) is a medical device manufactured by Osteogenics Biomedical Inc. This product is indexed under FDA Product Code / Category Classification NPL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZD1520TK
- Product Code / EMDN
- NPL
- Device Name
- Collagen Soft Tissue Matrix
- 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 ZDERM?
The registered manufacturer of record for ZDERM is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for ZDERM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZD1520TK.
What classification code is assigned to this device?
This device is registered under product classification code NPL.
Similar Classification Devices (NPL)
Other Devices by Osteogenics Biomedical Inc
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