← Back to catalogue

LabChoice Specimen Containers, Sterile, 90 mL

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
LabChoice Specimen Containers, Sterile, 90 mL FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
STERILE-EO FDA UDI
Model / Reference
43023 FDA UDI
Description
STERILE-EO FDA UDI

Identifiers

Primary DI / UDI-DI
00840117329447 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
General specimen container IVD, no additive/medium 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen container IVD, no additive/medium

LabChoice Specimen Containers, Sterile, 90 mL by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

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
Dynarex Corp.

Sources (1)

  • FDA UDI 30133c3d-af4a-4416-8daa-959e686f1c68 33 fields · synced Jun 1, 2026