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L-Type HDL-C Reagent 1

FDA UDI

Class II (US FDA UDI)

by Fujifilm Wako Pure Chemical Corporation

Identity

Trade Name
L-Type HDL-C Reagent 1 FDA UDI
Generic Name
High density lipoprotein (HDL) cholesterol IVD, calibrator FDA UDI
Device Name
In-Vitro Diagnostic Use FDA UDI
Model / Reference
991-00101 FDA UDI
Description
In-Vitro Diagnostic Use FDA UDI

Identifiers

Catalog Number
991-00101 FDA UDI
Primary DI / UDI-DI
14987481164564 FDA UDI
510(k) Number
K963847 FDA UDI
FDA Product Code
JIS FDA UDI
GMDN Term
High density lipoprotein (HDL) cholesterol IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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: High density lipoprotein (HDL) cholesterol IVD, calibrator

L-Type HDL-C Reagent 1 by Fujifilm Wako Pure Chemical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as High density lipoprotein (HDL) cholesterol IVD, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab4608c8-77b9-4839-80fd-6287fabc4784 37 fields · synced May 30, 2026