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Phosphorous Reagent

FDA UDI

by Cliniqa Corporation

Identity

Trade Name
Phosphorous Reagent FDA UDI
Generic Name
Inorganic phosphate (PO43-) IVD, reagent FDA UDI
Device Name
Phosphorous Reagent FDA UDI
Model / Reference
R85168 FDA UDI
Description
Phosphorous Reagent FDA UDI

Identifiers

Primary DI / UDI-DI
00817238011117 FDA UDI
GMDN Term
Inorganic phosphate (PO43-) IVD, reagent FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Inorganic phosphate (PO43-) IVD, reagent

Phosphorous Reagent by Cliniqa Corporation — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inorganic phosphate (PO43-) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cliniqa Corporation

Sources (1)

  • FDA UDI ba1dc09f-7550-49a0-a14a-daeb308bfc2d 33 fields · synced May 30, 2026