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Rhinostics, Inc.

FDA UDI

Class I (US FDA UDI)

by Rhinostics Inc

Identity

Trade Name
Rhinostics, Inc. FDA UDI
Generic Name
Specimen container mailer, non-insulated FDA UDI
Device Name
Rhinostics Capped Transport Tube FDA UDI
Model / Reference
LVL-1000001 FDA UDI
Description
Rhinostics Capped Transport Tube FDA UDI

Identifiers

Primary DI / UDI-DI
00850042963012 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
Specimen container mailer, non-insulated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen container mailer, non-insulated

Rhinostics, Inc. by Rhinostics Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen container mailer, non-insulated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rhinostics Inc

Sources (1)

  • FDA UDI 8858dd02-1712-41af-bc71-ea03daf7691e 33 fields · synced May 30, 2026