Veress Needle 120mm (UDI 05051223000792)
Device Regulatory Overview
The Veress Needle 120mm (Model/Catalog Number: PS3700) is a medical device manufactured by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical Manufacturing Limited. This product is indexed under FDA Product Code / Category Classification K0104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PS3700
- Product Code / EMDN
- K0104
- Device Name
- Veress Needle
- Database Sync Date
- 2026-08-09 16:29:59
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 Veress Needle 120mm?
The registered manufacturer of record for Veress Needle 120mm is Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical Manufacturing Limited.
What is the Primary UDI-DI identifier for Veress Needle 120mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051223000792.
What classification code is assigned to this device?
This device is registered under product classification code K0104.
Similar Classification Devices (K0104)
Other Devices by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical Manufacturing Limited
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