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Elecsys AMH

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Elecsys AMH FDA UDI
Generic Name
Anti-Mullerian hormone (AMH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
08819319160 FDA UDI

Identifiers

Catalog Number
08819319160 FDA UDI
Primary DI / UDI-DI
07613336166284 FDA UDI
510(k) Number
K203757 FDA UDI
FDA Product Code
PQO FDA UDI
GMDN Term
Anti-Mullerian hormone (AMH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1092 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

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: Anti-Mullerian hormone (AMH) IVD, kit, enzyme immunoassay (EIA)

Elecsys AMH by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anti-Mullerian hormone (AMH) IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

K203757 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eb5979b5-12ca-4ea1-9f9e-36542178db36 34 fields · synced Jun 6, 2026