gudid
Primary ID: 070.008
Straumann Membrane Flex (UDI 070.008)
Manufactured by COLLAGEN MATRIX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Straumann Membrane Flex - Primary ID 070.008
Device Regulatory Overview
The Straumann Membrane Flex (Model/Catalog Number: 070.008) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification NPL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 070.008
- Product Code / EMDN
- NPL
- Device Name
- Collagen Membrane 15mm x 20mm
- Database Sync Date
- 2026-08-09 09:14:39
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 Straumann Membrane Flex?
The registered manufacturer of record for Straumann Membrane Flex is COLLAGEN MATRIX, INC..
What is the Primary UDI-DI identifier for Straumann Membrane Flex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 070.008.
What classification code is assigned to this device?
This device is registered under product classification code NPL.
Similar Classification Devices (NPL)
Other Devices by COLLAGEN MATRIX, INC.
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