eudamed_udi
Primary ID: 05060485271277
Limpet with Adult Ambidex Cuff (UDI 05060485271277)
Manufactured by GM Instruments Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Limpet with Adult Ambidex Cuff - Primary ID 05060485271277
Device Regulatory Overview
The Limpet with Adult Ambidex Cuff (Model/Catalog Number: 0292A) 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
- 0292A
- Product Code / EMDN
- Z1203020599
- Device Name
- Aneroid Sphygmomanometers
- Database Sync Date
- 2026-08-09 16:29:26
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 Limpet with Adult Ambidex Cuff?
The registered manufacturer of record for Limpet with Adult Ambidex Cuff is GM Instruments Ltd.
What is the Primary UDI-DI identifier for Limpet with Adult Ambidex Cuff?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060485271277.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020599.
Similar Classification Devices (Z1203020599)
Other Devices by GM Instruments Ltd
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