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The Aftermarket Group Pediatric Nebulizer

FDA UDI

Class II (US FDA UDI)

by Invacare Corp.

Identity

Trade Name
The Aftermarket Group Pediatric Nebulizer FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
TAG PEDIATRIC NEBULIZER, LADY BUG FDA UDI
Model / Reference
NBA02-A52 FDA UDI
Description
TAG PEDIATRIC NEBULIZER, LADY BUG FDA UDI

Identifiers

Catalog Number
NEB-LADYBUG FDA UDI
Primary DI / UDI-DI
00841447108023 FDA UDI
510(k) Number
K043238 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

The Aftermarket Group Pediatric Nebulizer by Invacare Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Invacare Corp.

Sources (1)

  • FDA UDI 360fddde-ba4b-4e32-b3d0-66cee1ca0b21 37 fields · synced Jun 8, 2026