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Inflation Device

FDA UDI

Class II (US FDA UDI)

by Valflux Group, Llc

Identity

Trade Name
INFLATION DEVICE FDA UDI
Generic Name
Catheter/overtube balloon inflator, single-use FDA UDI
Device Name
VGAI25C INFLATION DEVICE FDA UDI
Model / Reference
VGAI25C FDA UDI
Description
VGAI25C INFLATION DEVICE FDA UDI

Identifiers

Catalog Number
VGAI25C FDA UDI
Primary DI / UDI-DI
00850004162040 FDA UDI
510(k) Number
K170027 FDA UDI
FDA Product Code
MAV FDA UDI
GMDN Term
Catheter/overtube balloon inflator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Catheter/overtube balloon inflator, single-use

Inflation Device by Valflux Group, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catheter/overtube balloon inflator, single-use.

Cleared under the same submission

K170027 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Valflux Group, Llc

Sources (1)

  • FDA UDI 7db52b15-426f-4ca2-bc7a-9aa3f8617864 36 fields · synced Jun 8, 2026