eudamed_udi
Primary ID: 00813877013581
Wearever (UDI 00813877013581)
Manufactured by Prime Life Fibers Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wearever - Primary ID 00813877013581
Device Regulatory Overview
The Wearever (Model/Catalog Number: HDM200GRYSM) is a medical device manufactured by Prime Life Fibers Inc.. This product is indexed under FDA Product Code / Category Classification T04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HDM200GRYSM
- Product Code / EMDN
- T04010102
- Device Name
- HDM200
- Database Sync Date
- 2026-08-09 16:30:11
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 Wearever?
The registered manufacturer of record for Wearever is Prime Life Fibers Inc..
What is the Primary UDI-DI identifier for Wearever?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00813877013581.
What classification code is assigned to this device?
This device is registered under product classification code T04010102.
Similar Classification Devices (T04010102)
Other Devices by Prime Life Fibers Inc.
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