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PAPP-A AccuBind ELISA Test System - 192 Wells

FDA UDI

by Monobind, Inc.

Identity

Trade Name
PAPP-A AccuBind ELISA Test System - 192 Wells FDA UDI
Generic Name
Pregnancy-associated plasma protein-A2 (PAPP-A2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
12625-300 FDA UDI

Identifiers

Catalog Number
12625-300B FDA UDI
Primary DI / UDI-DI
00816870021010 FDA UDI
GMDN Term
Pregnancy-associated plasma protein-A2 (PAPP-A2) IVD, kit, enzyme immunoassay (EIA) 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

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: Pregnancy-associated plasma protein-A2 (PAPP-A2) IVD, kit, enzyme immunoassay (EIA)

PAPP-A AccuBind ELISA Test System - 192 Wells by Monobind, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pregnancy-associated plasma protein-A2 (PAPP-A2) 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 10cc53f2-5cc4-4cde-9280-38fc83ba60bd 36 fields · synced May 31, 2026