gudid
Primary ID: SPRING-CUT
SPRING-CUT (UDI SPRING-CUT)
Manufactured by STERYLAB SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPRING-CUT - Primary ID SPRING-CUT
Device Regulatory Overview
The SPRING-CUT (Model/Catalog Number: SPRING-CUT) is a medical device manufactured by STERYLAB SRL. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPRING-CUT
- Product Code / EMDN
- FCG
- Device Name
- Semiautomatic guillottine type instrum. for soft tissue biopsy 16G; 11cm
- Database Sync Date
- 2026-08-09 09:04:33
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 SPRING-CUT?
The registered manufacturer of record for SPRING-CUT is STERYLAB SRL.
What is the Primary UDI-DI identifier for SPRING-CUT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SPRING-CUT.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by STERYLAB SRL
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