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Floodlight MS U-Turn Test

FDA UDI

Class I (US FDA UDI)

by Roche Molecular Systems, Inc.

Identity

Trade Name
Floodlight MS U-Turn Test FDA UDI
Generic Name
Self-care monitoring/reporting software FDA UDI
Model / Reference
09342290001 FDA UDI

Identifiers

Catalog Number
09342290001 FDA UDI
Primary DI / UDI-DI
07613336193334 FDA UDI
FDA Product Code
GWW FDA UDI
GMDN Term
Self-care monitoring/reporting software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1030 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Self-care monitoring/reporting software

Floodlight MS U-Turn Test by Roche Molecular Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-care monitoring/reporting software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Roche Molecular Systems, Inc.

Sources (1)

  • FDA UDI 331124a3-8b8a-4f4a-ab28-1e837f12b221 33 fields · synced Jun 9, 2026