gudid
Primary ID: A/SKINPURE-SAMPLE
skinPure (UDI A/SKINPURE-SAMPLE)
Manufactured by NIHON KOHDEN CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for skinPure - Primary ID A/SKINPURE-SAMPLE
Device Regulatory Overview
The skinPure (Model/Catalog Number: A/SKINPURE-SAMPLE) is a medical device manufactured by NIHON KOHDEN CORPORATION. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A/SKINPURE-SAMPLE
- Product Code / EMDN
- GYB
- Device Name
- SKINPURE, 1 SAMPLE TUBE (SKIN PREPARATION GEL)
- Database Sync Date
- 2026-08-09 09:50:50
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 skinPure?
The registered manufacturer of record for skinPure is NIHON KOHDEN CORPORATION.
What is the Primary UDI-DI identifier for skinPure?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A/SKINPURE-SAMPLE.
What classification code is assigned to this device?
This device is registered under product classification code GYB.
Similar Classification Devices (GYB)
Other Devices by NIHON KOHDEN CORPORATION
Programmatic Export
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