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PTH Intact AccuBind ELISA Test System - 96 Wells

FDA UDI

Class II (US FDA UDI)

by Monobind, Inc.

Identity

Trade Name
PTH Intact AccuBind ELISA Test System - 96 Wells FDA UDI
Generic Name
Parathyroid hormone (PTH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
9025-300 FDA UDI

Identifiers

Catalog Number
9025-300A FDA UDI
Primary DI / UDI-DI
00816870020402 FDA UDI
FDA Product Code
CEW FDA UDI
GMDN Term
Parathyroid hormone (PTH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1545 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: Parathyroid hormone (PTH) IVD, kit, enzyme immunoassay (EIA)

PTH Intact AccuBind ELISA Test System - 96 Wells by Monobind, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Parathyroid hormone (PTH) 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 1b37b194-dd0a-4cb6-97ad-0dd2bc547275 36 fields · synced May 30, 2026