12 Pneumatic Endo probes for Endo PAT 2000 (UDI 12 Pneumatic Endo probes for Endo PAT 2000)
Manufactured by ITAMAR MEDICAL LTD
Device Regulatory Overview
The 12 Pneumatic Endo probes for Endo PAT 2000 (Model/Catalog Number: 12 Pneumatic Endo probes for Endo PAT 2000) is a medical device manufactured by ITAMAR MEDICAL LTD. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12 Pneumatic Endo probes for Endo PAT 2000
- Product Code / EMDN
- DQK
- Device Name
- 12 Pneumatic Endo probes
- Database Sync Date
- 2026-08-09 09:18:13
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 12 Pneumatic Endo probes for Endo PAT 2000?
The registered manufacturer of record for 12 Pneumatic Endo probes for Endo PAT 2000 is ITAMAR MEDICAL LTD.
What is the Primary UDI-DI identifier for 12 Pneumatic Endo probes for Endo PAT 2000?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12 Pneumatic Endo probes for Endo PAT 2000.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by ITAMAR MEDICAL LTD
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