← Back to catalogue

Medical Action Industries

FDA UDI

Class I (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
General specimen container IVD, no additive, sterile FDA UDI
Device Name
Vial Clear w/ Cap VWR 50/Cs Pilot FDA UDI
Model / Reference
75543 FDA UDI
Description
Vial Clear w/ Cap VWR 50/Cs Pilot FDA UDI

Identifiers

Primary DI / UDI-DI
10809160002445 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
General specimen container IVD, no additive, sterile 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

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

Yes

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: General specimen container IVD, no additive, sterile

Medical Action Industries by Medical Action Industries Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive, sterile.

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
Medical Action Industries Inc.

Sources (1)

  • FDA UDI b384d763-7d2c-4bae-8b60-af355e1baf77 34 fields · synced May 30, 2026