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Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Urine specimen collection/transfer container IVD FDA UDI
Device Name
SPECIMEN PAN, DELUXE, WHITE, 40 OZ, DIAGONAL PLACEMENT GRADUATIONS, LATEX FREE, 100EA/CS FDA UDI
Model / Reference
MRT800 FDA UDI
Description
SPECIMEN PAN, DELUXE, WHITE, 40 OZ, DIAGONAL PLACEMENT GRADUATIONS, LATEX FREE, 100EA/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00840216127753 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
Urine specimen collection/transfer container IVD 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

Yes

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

Category: Urine specimen collection/transfer container IVD

Asp Medical by Asp Global, 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
Asp Global, LLC

Sources (1)

  • FDA UDI c9ac8fa2-9756-4e89-b1db-0a4d1955b058 33 fields · synced May 30, 2026