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Yodoc 10

FDA UDI

Class II (US FDA UDI)

by Dfi Co., Ltd

Identity

Trade Name
Yodoc 10 FDA UDI
Generic Name
Multiple urine analyte IVD, kit, rapid colorimetric, clinical FDA UDI
Device Name
The one device that DI number included 100 strips FDA UDI
Model / Reference
0024 FDA UDI
Description
The one device that DI number included 100 strips FDA UDI

Identifiers

Primary DI / UDI-DI
08806141301998 FDA UDI
FDA Product Code
JIL FDA UDI
JIO FDA UDI
JIR FDA UDI
LJX FDA UDI
JMT FDA UDI
CDM FDA UDI
CEN FDA UDI
JRE FDA UDI
JIN FDA UDI
JJB FDA UDI
GMDN Term
Multiple urine analyte IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1340 FDA UDI
864.6550 FDA UDI
862.1645 FDA UDI
864.7675 FDA UDI
862.1510 FDA UDI
862.1785 FDA UDI
862.1550 FDA UDI
862.2800 FDA UDI
862.1435 FDA UDI
862.1115 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

Yes

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

No

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, kit, rapid colorimetric, clinical

Yodoc 10 by Dfi Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, kit, rapid colorimetric, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dfi Co., Ltd

Sources (1)

  • FDA UDI 1955d844-c40e-482e-ab99-26570f029bc7 34 fields · synced May 29, 2026