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KOVA Plastics Urinalysis System

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 87141E

by Alltrista Plastics LLC

Identity

Trade Name
Kova Plastics FDA UDI
Generic Name
Test tube/reservoir cap FDA UDI
Device Name
KOVA Plastics Urinalysis System EUDAMED
Kova Ko-Lec-Pac (Urinalysis package containing 500 plastic tubes, 500 plastic caps, 500 plastic cups, and 500 labels) FDA UDI
Model / Reference
87141E EUDAMED
87141 FDA UDI
Description
Kova Ko-Lec-Pac (Urinalysis package containing 500 plastic tubes, 500 plastic caps, 500 plastic cups, and 500 labels) FDA UDI

Identifiers

Catalog Number
87141 / 87141E FDA UDI
Primary DI / UDI-DI
00850033297119 EUDAMEDFDA UDI
Basic UDI-DI
0850033297KOVAPLASTICSF5 EUDAMED
Direct Marketing DI
00850033297119 EUDAMED
FDA Product Code
NNK FDA UDI
EMDN Code
W05010202,W05010280,W0503020199,W0503900202 EUDAMED
GMDN Term
Test tube/reservoir cap FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

KOVA Plastics Urinalysis System by Alltrista Plastics LLC — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000021674
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED db6d32b2-3df6-47b8-bfef-78dcc4c85ab5 61 fields · synced Jun 19, 2026
  • FDA UDI 3b70c632-c410-429a-8b9f-bccdb7ae1f10 36 fields · synced May 30, 2026