eudamed_udi
Primary ID: +G399CTL2S0+
Periotome (UDI +G399CTL2S0+)
Manufactured by CROSSTEX (PRIVATE) LIMITED.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Periotome - Primary ID +G399CTL2S0+
Device Regulatory Overview
The Periotome (Model/Catalog Number: CT-L2S) is a medical device manufactured by CROSSTEX (PRIVATE) LIMITED.. This product is indexed under FDA Product Code / Category Classification Q010399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CT-L2S
- Product Code / EMDN
- Q010399
- Device Name
- Periotome
- Database Sync Date
- 2026-08-09 16:49:22
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 Periotome?
The registered manufacturer of record for Periotome is CROSSTEX (PRIVATE) LIMITED..
What is the Primary UDI-DI identifier for Periotome?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G399CTL2S0+.
What classification code is assigned to this device?
This device is registered under product classification code Q010399.
Similar Classification Devices (Q010399)
Other Devices by CROSSTEX (PRIVATE) LIMITED.
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