PULSE OXIMETERS (UDI Z1203020408)
Device Regulatory Overview
The PULSE OXIMETERS (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Z1203020408 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Z1203020408
- Device Name
- PULSE OXIMETERS
- Database Sync Date
- 2026-08-09 16:18:37
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 PULSE OXIMETERS?
The registered manufacturer of record for PULSE OXIMETERS is .
What is the Primary UDI-DI identifier for PULSE OXIMETERS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z1203020408.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020408.
Similar Classification Devices (Z1203020408)
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