Identity

Trade Name
Nebulizer Kit FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
Sunset SperaChamber - 50/pack FDA UDI
Model / Reference
RES195-50 FDA UDI
Description
Sunset SperaChamber - 50/pack FDA UDI

Identifiers

Primary DI / UDI-DI
00848530098575 FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop FDA UDI

Classification

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

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Nebulizer Kit by SUNSET HEALTHCARE SOLUTIONS, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4501e218-adca-4e76-9549-9063c34534e9 34 fields · synced Jun 1, 2026