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urinalysis strips

FDA UDI

Class I (US FDA UDI)

by Weihai Kangzheng Medical Equipment Technology Co., Ltd

Identity

Trade Name
urinalysis strips FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Model / Reference
3T FDA UDI

Identifiers

Primary DI / UDI-DI
06971257037177 FDA UDI
FDA Product Code
LJX FDA UDI
JMT FDA UDI
CEN FDA UDI
GMDN Term
Multiple urine analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.7675 FDA UDI
862.1510 FDA UDI
862.1550 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

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

Yes

FDA UDI

Category: Multiple urine analyte IVD, control

urinalysis strips by Weihai Kangzheng Medical Equipment Technology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 666f5650-46f4-41a4-a5e3-716da2ba9ef8 32 fields · synced May 30, 2026