gudid
Primary ID: 20x25mm
Cytoflex Resorb (UDI 20x25mm)
Manufactured by UNICARE BIOMEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cytoflex Resorb - Primary ID 20x25mm
Device Regulatory Overview
The Cytoflex Resorb (Model/Catalog Number: 20x25mm) is a medical device manufactured by UNICARE BIOMEDICAL INC.. This product is indexed under FDA Product Code / Category Classification NPK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20x25mm
- Product Code / EMDN
- NPK
- Device Name
- Cytoflex Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex Resorb barriers are resorbable and do not require a second retrieval procedure.
- 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 Cytoflex Resorb?
The registered manufacturer of record for Cytoflex Resorb is UNICARE BIOMEDICAL INC..
What is the Primary UDI-DI identifier for Cytoflex Resorb?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20x25mm.
What classification code is assigned to this device?
This device is registered under product classification code NPK.
Similar Classification Devices (NPK)
Other Devices by UNICARE BIOMEDICAL INC.
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