proGAV 2.0®

FDA UDI

Class II (US FDA UDI)

by Christoph Miethke GmbH & Co. KG

Identity

Trade Name: proGAV 2.0® FDA UDI
Generic Name: Cerebrospinal fluid shunt valve programmer FDA UDI
Device Name: PROGAV 2.0 TOOL SET EXTENDED FDA UDI
Model / Reference: FX499T FDA UDI
Description: PROGAV 2.0 TOOL SET EXTENDED FDA UDI

Identifiers

Catalog Number: FX499T FDA UDI
Primary DI / UDI-DI: 04041906141714 FDA UDI
FDA Product Code: JXG FDA UDI
GMDN Term: Cerebrospinal fluid shunt valve programmer 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Cerebrospinal fluid shunt valve programmer

proGAV 2.0® by Christoph Miethke GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Christoph Miethke GmbH & Co. KG

Sources (1)

FDA UDI 4993513d-798a-4102-a7a8-4b426d4b2471 35 fields · synced May 30, 2026