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RightSpotpH®

FDA UDI

Class I (US FDA UDI)

by Rightbio/Metrics Inc.

Identity

Trade Name
RightSpotpH® FDA UDI
Generic Name
pH meter IVD FDA UDI
Device Name
Small Bore Indicator FDA UDI
Model / Reference
RSSB001 FDA UDI
Description
Small Bore Indicator FDA UDI

Identifiers

Primary DI / UDI-DI
00861145002607 FDA UDI
FDA Product Code
JLL FDA UDI
GMDN Term
pH meter IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: pH meter IVD

RightSpotpH® by Rightbio/Metrics Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as pH meter IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1560e996-55f1-41b4-b42a-1774f72968ab 35 fields · synced May 30, 2026