gudid
Primary ID: 4334
Pulmo-Mist Compressor (UDI 4334)
Manufactured by NIDEK MEDICAL PRODUCTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pulmo-Mist Compressor - Primary ID 4334
Device Regulatory Overview
The Pulmo-Mist Compressor (Model/Catalog Number: 4334) is a medical device manufactured by NIDEK MEDICAL PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4334
- Product Code / EMDN
- BTI
- Device Name
- Database Sync Date
- 2026-08-09 09:08:52
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 Pulmo-Mist Compressor?
The registered manufacturer of record for Pulmo-Mist Compressor is NIDEK MEDICAL PRODUCTS, INC..
What is the Primary UDI-DI identifier for Pulmo-Mist Compressor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4334.
What classification code is assigned to this device?
This device is registered under product classification code BTI.
Similar Classification Devices (BTI)
Other Devices by NIDEK MEDICAL PRODUCTS, INC.
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