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BodyMed

FDA UDI

Class II (US FDA UDI)

by Boxout, Llc

Identity

Trade Name
BodyMed FDA UDI
Generic Name
Nebulizing system delivery set, single-use FDA UDI
Device Name
BODYMED NEBULIZER KIT WITH PEDIATRIC MASK, INCLUDING A DISPOSABLE PEDIATRIC MASK, 6CC MEDICATION CUP, AND TUBING. FDA UDI
Model / Reference
BDMNEBPMK FDA UDI
Description
BODYMED NEBULIZER KIT WITH PEDIATRIC MASK, INCLUDING A DISPOSABLE PEDIATRIC MASK, 6CC MEDICATION CUP, AND TUBING. FDA UDI

Identifiers

Primary DI / UDI-DI
00815991024672 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, single-use 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nebulizing system delivery set, single-use

BodyMed by Boxout, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boxout, Llc

Sources (1)

  • FDA UDI b6c68198-05c8-4415-83f6-aadcbede916d 33 fields · synced May 30, 2026