eudamed_udi
Primary ID: 08680829214172
KNEE PACK (UDI 08680829214172)
Manufactured by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KNEE PACK - Primary ID 08680829214172
Device Regulatory Overview
The KNEE PACK (Model/Catalog Number: 8880424) is a medical device manufactured by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification T0202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8880424
- Product Code / EMDN
- T0202
- Device Name
- STERILE DISPOSABLE SURGICAL GOWNS Small
- Database Sync Date
- 2026-08-09 16:28:50
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 KNEE PACK?
The registered manufacturer of record for KNEE PACK is MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ.
What is the Primary UDI-DI identifier for KNEE PACK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680829214172.
What classification code is assigned to this device?
This device is registered under product classification code T0202.
Similar Classification Devices (T0202)
Other Devices by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ
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