eudamed_udi
Primary ID: 00889024375178
PULSAVAC® (UDI 00889024375178)
Manufactured by Zimmer Surgical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PULSAVAC® - Primary ID 00889024375178
Device Regulatory Overview
The PULSAVAC® (Model/Catalog Number: 00-5150-476-01) is a medical device manufactured by Zimmer Surgical, Inc.. This product is indexed under FDA Product Code / Category Classification A03040299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00-5150-476-01
- Product Code / EMDN
- A03040299
- Device Name
- Wound Debridement (AC Powered Pulsavac)
- Database Sync Date
- 2026-08-09 16:29:23
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 PULSAVAC®?
The registered manufacturer of record for PULSAVAC® is Zimmer Surgical, Inc..
What is the Primary UDI-DI identifier for PULSAVAC®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00889024375178.
What classification code is assigned to this device?
This device is registered under product classification code A03040299.
Similar Classification Devices (A03040299)
Other Devices by Zimmer Surgical, Inc.
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