gudid
Primary ID: 615.03.01S
CRANIOS Reinforced (UDI 615.03.01S)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CRANIOS Reinforced - Primary ID 615.03.01S
Device Regulatory Overview
The CRANIOS Reinforced (Model/Catalog Number: 615.03.01S) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification GXP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 615.03.01S
- Product Code / EMDN
- GXP
- Device Name
- CRANIOS REINFORCED FAST SET PUTTY 3CC-STERILE
- Database Sync Date
- 2026-08-09 09:39:06
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 CRANIOS Reinforced?
The registered manufacturer of record for CRANIOS Reinforced is Synthes GmbH.
What is the Primary UDI-DI identifier for CRANIOS Reinforced?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 615.03.01S.
What classification code is assigned to this device?
This device is registered under product classification code GXP.
Similar Classification Devices (GXP)
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