Duplex Aneroid Large Adult Ambidex Cuff (UDI 05060485271246)
Manufactured by GM Instruments Ltd
Device Regulatory Overview
The Duplex Aneroid Large Adult Ambidex Cuff (Model/Catalog Number: 0329A) is a medical device manufactured by GM Instruments Ltd. This product is indexed under FDA Product Code / Category Classification Z1203020599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0329A
- Product Code / EMDN
- Z1203020599
- Device Name
- Aneroid Sphygmomanometers
- Database Sync Date
- 2026-08-09 16:30:37
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 Duplex Aneroid Large Adult Ambidex Cuff?
The registered manufacturer of record for Duplex Aneroid Large Adult Ambidex Cuff is GM Instruments Ltd.
What is the Primary UDI-DI identifier for Duplex Aneroid Large Adult Ambidex Cuff?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060485271246.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020599.
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