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Asp Medical

FDA UDI

Class II (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Sputum specimen container IVD FDA UDI
Device Name
SPECIMEN TRAP 40CC, W/ TRANSPORT CAP, STERILE FDA UDI
Model / Reference
MRT441 FDA UDI
Description
SPECIMEN TRAP 40CC, W/ TRANSPORT CAP, STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00840216101661 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Sputum specimen container IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sputum specimen container IVD

Asp Medical by Asp Global, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sputum specimen container IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI db64bf56-468e-4b2c-97d1-6b0b0418a2a8 33 fields · synced May 31, 2026