← Back to catalogue

Aero-Med

FDA UDI

Class I (US FDA UDI)

by Aero-Med Llc

Identity

Trade Name
Aero-Med FDA UDI
Generic Name
General specimen collection kit IVD, clinical FDA UDI
Device Name
Viral Transport Kit, Nasopharyngeal Swab, 3mL VTM FDA UDI
Model / Reference
CA40000 FDA UDI
Description
Viral Transport Kit, Nasopharyngeal Swab, 3mL VTM FDA UDI

Identifiers

Catalog Number
CA40000 FDA UDI
Primary DI / UDI-DI
10885380184208 FDA UDI
FDA Product Code
OIB FDA UDI
GMDN Term
General specimen collection kit IVD, clinical 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen collection kit IVD, clinical

Aero-Med by Aero-Med Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen collection kit IVD, clinical.

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

Manufacturer
Aero-Med Llc

Sources (1)

  • FDA UDI f6503d96-c9ce-44b2-a23d-103b96d95d6b 34 fields · synced Jun 8, 2026