BioWrap (UDI 17-04-155714)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BioWrap (Model/Catalog Number: 17-04-155714) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 17-04-155714
Product Code / EMDN: GYB
Device Name: BioWrap Conductive Cream
Database Sync Date: 2026-08-09 09:49:29

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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Frequently Asked Questions

Who is the primary manufacturer of BioWrap?

The registered manufacturer of record for BioWrap is PARKER LABORATORIES INC.

What is the Primary UDI-DI identifier for BioWrap?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 17-04-155714.

What classification code is assigned to this device?

This device is registered under product classification code GYB.

Similar Classification Devices (GYB)

Other Devices by PARKER LABORATORIES INC

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