gudid
Primary ID: ZF200
ZCORE FORM (UDI ZF200)
Manufactured by Osteogenics Biomedical Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZCORE FORM - Primary ID ZF200
Device Regulatory Overview
The ZCORE FORM (Model/Catalog Number: ZF200) is a medical device manufactured by Osteogenics Biomedical Inc. This product is indexed under FDA Product Code / Category Classification NPM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZF200
- Product Code / EMDN
- NPM
- Device Name
- Moldable Collagen-Enriched Porcine Xenograft, Particle Size 0.25-1.0 mm, Sterile, Contents: 2.0 cc
- 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 ZCORE FORM?
The registered manufacturer of record for ZCORE FORM is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for ZCORE FORM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZF200.
What classification code is assigned to this device?
This device is registered under product classification code NPM.
Similar Classification Devices (NPM)
Other Devices by Osteogenics Biomedical Inc
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