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Kova Plastics

FDA UDI

Class I (US FDA UDI)

by Alltrista Plastics LLC

Identity

Trade Name
Kova Plastics FDA UDI
Generic Name
Test tube/reservoir cap FDA UDI
Device Name
Kova POC Urinalysis System Pac (Urinalysis package containing 100 plastic tubes, 100 plastic tube caps, 100 plastic pipettes, and 10 10-chambered plastic microscope slides with gridlines) FDA UDI
Model / Reference
88100 FDA UDI
Description
Kova POC Urinalysis System Pac (Urinalysis package containing 100 plastic tubes, 100 plastic tube caps, 100 plastic pipettes, and 10 10-chambered plastic microscope slides with gridlines) FDA UDI

Identifiers

Catalog Number
88100 FDA UDI
Primary DI / UDI-DI
00850033297188 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
Test tube/reservoir cap 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

No

FDA UDI

Category: General specimen microscopy slide IVD, single-useCentrifuge tube IVDTest tube/reservoir capUser-induced pipette

Kova Plastics by Alltrista Plastics LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as User-induced pipette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c234aed-aaa4-492e-8a3c-57579bedfd21 36 fields · synced Jun 8, 2026