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KOVA Plastics Urinalysis System
EUDAMEDFDA UDIClass A (EU MDR)
Ref 87144FRef 87162E
Identity
- Trade Name
- Kova Plastics FDA UDI
- Generic Name
- Centrifuge tube IVD FDA UDI
- Device Name
- KOVA Plastics Urinalysis System EUDAMEDKova Plastics Super System Pac 1000 with Grid (Urinalysis package containing 1000 plastic tubes, 1000 plastic pipettes, and 100 10-chambered microscope slides with gridlines) FDA UDI
- Model / Reference
- 87144F EUDAMED87162E EUDAMED87162 FDA UDI
- Description
- Kova Plastics Super System Pac 1000 with Grid (Urinalysis package containing 1000 plastic tubes, 1000 plastic pipettes, and 100 10-chambered microscope slides with gridlines) FDA UDI
Identifiers
- Catalog Number
- 87162 / 87162E FDA UDI
- Primary DI / UDI-DI
- 00850033297256 EUDAMED00850033297089 EUDAMEDFDA UDI
- Basic UDI-DI
- 0850033297KOVAPLASTICSF5 EUDAMED
- Direct Marketing DI
- 00850033297256 EUDAMED00850033297089 EUDAMED
- FDA Product Code
- NNW FDA UDI
- EMDN Code
- W0503900202 MICROSCOPE SLIDES COVERSLIP EUDAMEDW05010202,W0503020199,W0503900202 EUDAMED
- GMDN Term
- Centrifuge tube IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 876.5250 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 0850033297KOVAPLASTICSF5 | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Alltrista Plastics LLC
- EUDAMED SRN
- US-MF-000021674
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (3)
- EUDAMED 5f78ffac-52b2-44dd-96dc-1899ba7c4415 61 fields · synced Jul 14, 2026
- EUDAMED eb5a634c-a54b-4d9b-bc01-4329254b1341 61 fields · synced May 16, 2026
- FDA UDI 0177a531-18c8-4fdd-9faf-2425661c9188 36 fields · synced May 30, 2026