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IL-6 AccuLite CLIA Test System - 192 Wells

FDA UDI

Class N (US FDA UDI)

by Monobind, Inc.

Identity

Trade Name
IL-6 AccuLite CLIA Test System - 192 Wells FDA UDI
Generic Name
Interleukin-6 receptor (IL-6r) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
13275-300 FDA UDI

Identifiers

Catalog Number
13275-300B FDA UDI
Primary DI / UDI-DI
00816870023984 FDA UDI
FDA Product Code
QLC FDA UDI
GMDN Term
Interleukin-6 receptor (IL-6r) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
N FDA UDI
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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 7.75 Inch FDA UDI

Category: Interleukin-6 receptor (IL-6r) IVD, kit, enzyme immunoassay (EIA)

IL-6 AccuLite CLIA Test System - 192 Wells by Monobind, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interleukin-6 receptor (IL-6r) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Monobind, Inc.

Sources (1)

  • FDA UDI 024665ee-52c7-43b1-b8dc-fd363ae22397 36 fields · synced May 31, 2026