gudid
Primary ID: EMAST21WSB
EMA (UDI EMAST21WSB)
Manufactured by The Myerson Company Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EMA - Primary ID EMAST21WSB
Device Regulatory Overview
The EMA (Model/Catalog Number: EMAST21WSB) is a medical device manufactured by The Myerson Company Limited. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EMAST21WSB
- Product Code / EMDN
- LRK
- Device Name
- EMA Strap 21mm White/Soft Bulk
- Database Sync Date
- 2026-08-09 09:16:45
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 EMA?
The registered manufacturer of record for EMA is The Myerson Company Limited.
What is the Primary UDI-DI identifier for EMA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EMAST21WSB.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
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