Identity
- Trade Name
- PROGAV 2.0 FDA UDI
- Generic Name
- Ventriculo-peritoneal/atrial shunt FDA UDI
- Device Name
- PROGAV 2.0 SYS SA2.0 30 & PRECHAMBER FDA UDI
- Model / Reference
- FX592T FDA UDI
- Description
- PROGAV 2.0 SYS SA2.0 30 & PRECHAMBER FDA UDI
Identifiers
- Catalog Number
- FX592T FDA UDI
- Primary DI / UDI-DI
- 04041906503062 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Ventriculo-peritoneal/atrial shunt FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5550 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ventriculo-peritoneal/atrial shunt
Progav 2.0 by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ventriculo-peritoneal/atrial shunt.
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- CODMAN® HAKIM® — Integra LifeSciences Production Corporation · Class II
- AESCULAP — Christoph Miethke GmbH & Co. KG · Class II
- proGAV 2.0® — Christoph Miethke GmbH & Co. KG · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI c05ce77d-47b5-4054-b88c-5d129ca44957 35 fields · synced May 30, 2026