GramaDerm (UDI 07503006698811)
Manufactured by Oculus Technologies of México S.A. de C.V.
Device Regulatory Overview
The GramaDerm (Model/Catalog Number: P-E112T00) is a medical device manufactured by Oculus Technologies of México S.A. de C.V.. This product is indexed under FDA Product Code / Category Classification M04040501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P-E112T00
- Product Code / EMDN
- M04040501
- Device Name
- GramaDerm Combo-Pack
- Database Sync Date
- 2026-08-09 16:50:07
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 GramaDerm?
The registered manufacturer of record for GramaDerm is Oculus Technologies of México S.A. de C.V..
What is the Primary UDI-DI identifier for GramaDerm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07503006698811.
What classification code is assigned to this device?
This device is registered under product classification code M04040501.
Similar Classification Devices (M04040501)
Other Devices by Oculus Technologies of México S.A. de C.V.
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