AK-ML-TP Femoral Stem (132°) (UDI 06943735134739)
Manufactured by Beijing AK Medical Co., Ltd.
Device Regulatory Overview
The AK-ML-TP Femoral Stem (132°) (Model/Catalog Number: 1100-2845) is a medical device manufactured by Beijing AK Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification P090804010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1100-2845
- Product Code / EMDN
- P090804010202
- Device Name
- AK-ML-TP Femoral Stem (132°)
- Database Sync Date
- 2026-08-09 16:30:39
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 AK-ML-TP Femoral Stem (132°)?
The registered manufacturer of record for AK-ML-TP Femoral Stem (132°) is Beijing AK Medical Co., Ltd..
What is the Primary UDI-DI identifier for AK-ML-TP Femoral Stem (132°)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06943735134739.
What classification code is assigned to this device?
This device is registered under product classification code P090804010202.
Similar Classification Devices (P090804010202)
Other Devices by Beijing AK Medical Co., Ltd.
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