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Green Sprouts

FDA UDI

Class I (US FDA UDI)

by O2cool, LLC

Identity

Trade Name
Green Sprouts FDA UDI
Generic Name
Nasal aspirator, manual FDA UDI
Device Name
Sprout Ware® Nasal Aspirator made from Plants and Silicone-Tube-Green-Adult Use Only FDA UDI
Model / Reference
309305-500-00 FDA UDI
Description
Sprout Ware® Nasal Aspirator made from Plants and Silicone-Tube-Green-Adult Use Only FDA UDI

Identifiers

Primary DI / UDI-DI
00715418176833 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Nasal aspirator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
Commercial Distribution
Not 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

No

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

Green Sprouts by O2cool, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
O2cool, LLC

Sources (1)

  • FDA UDI 027eceee-4c3f-4fc4-8f3d-2a86a923d7ea 34 fields · synced May 30, 2026