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Cortisol AccuLite CLIA Test System - 96 Wells

FDA UDI

Class II (US FDA UDI)

by Monobind, Inc.

Identity

Trade Name
Cortisol AccuLite CLIA Test System - 96 Wells FDA UDI
Generic Name
Total cortisol IVD, kit, chemiluminescent immunoassay FDA UDI
Model / Reference
3675-300 FDA UDI

Identifiers

Catalog Number
3675-300A FDA UDI
Primary DI / UDI-DI
00816870022758 FDA UDI
FDA Product Code
CGR FDA UDI
GMDN Term
Total cortisol IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1205 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

Yes

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: Total cortisol IVD, kit, chemiluminescent immunoassay

Cortisol AccuLite CLIA Test System - 96 Wells by Monobind, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total cortisol IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Monobind, Inc.

Sources (1)

  • FDA UDI e0b44aab-d393-49ed-b022-c5830dc1546e 36 fields · synced Jun 8, 2026