gudid
Primary ID: 25x30mm
Perforated Tefguard (UDI 25x30mm)
Manufactured by UNICARE BIOMEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perforated Tefguard - Primary ID 25x30mm
Device Regulatory Overview
The Perforated Tefguard (Model/Catalog Number: 25x30mm) is a medical device manufactured by UNICARE BIOMEDICAL INC.. This product is indexed under FDA Product Code / Category Classification LYC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 25x30mm
- Product Code / EMDN
- LYC
- Device Name
- Perforated Tefguard membranes are made of the same materials and features as Cytoflex Tefguard membranes with the exception of perforation. The perforated macro holes allow for direct vascularization across the membrane. Both the Cytoflex Tefguard and Perforated Tefguard membranes are designed to achieve predictable outcomes for GBR procedures.
- 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Perforated Tefguard?
The registered manufacturer of record for Perforated Tefguard is UNICARE BIOMEDICAL INC..
What is the Primary UDI-DI identifier for Perforated Tefguard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25x30mm.
What classification code is assigned to this device?
This device is registered under product classification code LYC.
Similar Classification Devices (LYC)
Other Devices by UNICARE BIOMEDICAL INC.
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