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BOEHRINGER® High Flow Bubble Barb

FDA UDI

Class II (US FDA UDI)

by Boehringer Laboratories, Llc

Identity

Trade Name
BOEHRINGER® High Flow Bubble Barb FDA UDI
Generic Name
Vacuum suction regulator/regulation set, general-purpose FDA UDI
Device Name
High Flow Bubble Barb FDA UDI
Model / Reference
2469 FDA UDI
Description
High Flow Bubble Barb FDA UDI

Identifiers

Catalog Number
2469 FDA UDI
Primary DI / UDI-DI
10816286020482 FDA UDI
FDA Product Code
KDP FDA UDI
GMDN Term
Vacuum suction regulator/regulation set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vacuum suction regulator/regulation set, general-purpose

BOEHRINGER® High Flow Bubble Barb by Boehringer Laboratories, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum suction regulator/regulation set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boehringer Laboratories, Llc

Sources (1)

  • FDA UDI ebec68dd-080a-4fa0-b97f-50517bb942dd 35 fields · synced Jun 6, 2026