← Back to catalogue

Chloride LiquiColor®

FDA UDI

Class II (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
Chloride LiquiColor® FDA UDI
Generic Name
Chloride (Cl-) IVD, kit, spectrophotometry FDA UDI
Device Name
Quantitative Colorimetric Determination of Chloride in Serum, Plasma, Urine and CSF. FDA UDI
Model / Reference
0210-250 FDA UDI
Description
Quantitative Colorimetric Determination of Chloride in Serum, Plasma, Urine and CSF. FDA UDI

Identifiers

Catalog Number
0210-250 FDA UDI
Primary DI / UDI-DI
00657498000632 FDA UDI
FDA Product Code
CHJ FDA UDI
GMDN Term
Chloride (Cl-) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1170 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

No

FDA UDI

Category: Chloride (Cl-) IVD, kit, spectrophotometry

Chloride LiquiColor® by Stanbio Laboratory, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 62a78c88-e853-4ecc-98f7-c3895e14cd5f 36 fields · synced Jun 1, 2026