gudid
Primary ID: AJ1832A-02/25
Intradermal Cannulae and Needles (UDI AJ1832A-02/25)
Manufactured by STERIMEDIX LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Intradermal Cannulae and Needles - Primary ID AJ1832A-02/25
Device Regulatory Overview
The Intradermal Cannulae and Needles (Model/Catalog Number: AJ1832A-02/25) is a medical device manufactured by STERIMEDIX LIMITED. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AJ1832A-02/25
- Product Code / EMDN
- MED
- Device Name
- Silkann(FT) Cann 22gx60mm
- Database Sync Date
- 2026-08-09 09:22:52
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 Intradermal Cannulae and Needles?
The registered manufacturer of record for Intradermal Cannulae and Needles is STERIMEDIX LIMITED.
What is the Primary UDI-DI identifier for Intradermal Cannulae and Needles?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AJ1832A-02/25.
What classification code is assigned to this device?
This device is registered under product classification code MED.
Similar Classification Devices (MED)
Other Devices by STERIMEDIX LIMITED
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