Spencer (UDI JM30021 SPECTAR FOAM CERVICAL COLLAR BIVALVE SIZE S)
Manufactured by SPENCER ITALIA SRL
Device Regulatory Overview
The Spencer (Model/Catalog Number: JM30021 SPECTAR FOAM CERVICAL COLLAR BIVALVE SIZE S) is a medical device manufactured by SPENCER ITALIA SRL. This product is indexed under FDA Product Code / Category Classification IQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- JM30021 SPECTAR FOAM CERVICAL COLLAR BIVALVE SIZE S
- Product Code / EMDN
- IQK
- Device Name
- Database Sync Date
- 2026-08-09 09:04:28
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 Spencer?
The registered manufacturer of record for Spencer is SPENCER ITALIA SRL.
What is the Primary UDI-DI identifier for Spencer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is JM30021 SPECTAR FOAM CERVICAL COLLAR BIVALVE SIZE S.
What classification code is assigned to this device?
This device is registered under product classification code IQK.
Similar Classification Devices (IQK)
Other Devices by SPENCER ITALIA SRL
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