gudid
Primary ID: PS1306
PressTo (UDI PS1306)
Manufactured by M.D.L. S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PressTo - Primary ID PS1306
Device Regulatory Overview
The PressTo (Model/Catalog Number: PS1306) is a medical device manufactured by M.D.L. S.R.L.. This product is indexed under FDA Product Code / Category Classification DWO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PS1306
- Product Code / EMDN
- DWO
- Device Name
- DISPOSABLE BONE MARROW BIOPSY NEEDLE WITH INTERNAL TRAP SYSTEM, SAFETY, WIRE 13G x 60 mm
- Database Sync Date
- 2026-08-09 09:04:30
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 PressTo?
The registered manufacturer of record for PressTo is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for PressTo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PS1306.
What classification code is assigned to this device?
This device is registered under product classification code DWO.
Similar Classification Devices (DWO)
Other Devices by M.D.L. S.R.L.
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