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Voluminous™

FDA UDI

Class II (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
Voluminous™ FDA UDI
Generic Name
Catheter/overtube balloon inflator, single-use FDA UDI
Device Name
40CC-15ATM VOLUMINOUS INFLATION DEVICE FDA UDI
Model / Reference
622513 FDA UDI
Description
40CC-15ATM VOLUMINOUS INFLATION DEVICE FDA UDI

Identifiers

Catalog Number
622513 FDA UDI
Primary DI / UDI-DI
04046964539022 FDA UDI
FDA Product Code
MAV FDA UDI
KOE 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
876.5520 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Catheter/overtube balloon inflator, single-use

Voluminous™ by B Braun Interventional Systems, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B Braun Interventional Systems, Inc

Sources (1)

  • FDA UDI 86c06ca6-9c60-45cf-9333-26d5e17e4323 36 fields · synced Jun 8, 2026