BioStep PRO, Size 23, Left, Rate 32, Dark (UDI 00713980024484)
Manufactured by Alps South, LLC
Device Regulatory Overview
The BioStep PRO, Size 23, Left, Rate 32, Dark (Model/Catalog Number: BSPRO-23L-32D) is a medical device manufactured by Alps South, LLC. This product is indexed under FDA Product Code / Category Classification Y062499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BSPRO-23L-32D
- Product Code / EMDN
- Y062499
- Device Name
- BIOSTEP PRO
- Database Sync Date
- 2026-08-09 16:28:51
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 BioStep PRO, Size 23, Left, Rate 32, Dark?
The registered manufacturer of record for BioStep PRO, Size 23, Left, Rate 32, Dark is Alps South, LLC.
What is the Primary UDI-DI identifier for BioStep PRO, Size 23, Left, Rate 32, Dark?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00713980024484.
What classification code is assigned to this device?
This device is registered under product classification code Y062499.
Similar Classification Devices (Y062499)
Other Devices by Alps South, LLC
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