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Vive Breathe

FDA UDI

Class II (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
Vive Breathe FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
Compressor Nebulizer Accessories (Pediatric Mask, Resuable) FDA UDI
Model / Reference
LVA3077MSKRC FDA UDI
Description
Compressor Nebulizer Accessories (Pediatric Mask, Resuable) FDA UDI

Identifiers

Primary DI / UDI-DI
00810178882953 FDA UDI
510(k) Number
K161586 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nebulizing system delivery set, reusable

Vive Breathe by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vive Health Llc

Sources (1)

  • FDA UDI 70c02205-3c2f-489a-9778-c10a48c57699 34 fields · synced May 30, 2026