PLASTIC SPECTACLE FRAMES WITHOUT LENSES (UDI Q02100202)
Device Regulatory Overview
The PLASTIC SPECTACLE FRAMES WITHOUT LENSES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Q02100202
- Device Name
- PLASTIC SPECTACLE FRAMES WITHOUT LENSES
- Database Sync Date
- 2026-08-09 16:18:37
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 PLASTIC SPECTACLE FRAMES WITHOUT LENSES?
The registered manufacturer of record for PLASTIC SPECTACLE FRAMES WITHOUT LENSES is .
What is the Primary UDI-DI identifier for PLASTIC SPECTACLE FRAMES WITHOUT LENSES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Q02100202.
What classification code is assigned to this device?
This device is registered under product classification code Q02100202.
Similar Classification Devices (Q02100202)
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