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RAPIDLab® 1200 pH Electrode Fill

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
RAPIDLab® 1200 pH Electrode Fill FDA UDI
Generic Name
Hydrogen (H+)/pH electrode IVD FDA UDI
Device Name
pH electrode fill soultion, in vitro diagnostics material for use with RAPIDLab® 1200 series electrodes FDA UDI
Model / Reference
10376881 FDA UDI
Description
pH electrode fill soultion, in vitro diagnostics material for use with RAPIDLab® 1200 series electrodes FDA UDI

Identifiers

Catalog Number
10376881 FDA UDI
Primary DI / UDI-DI
00630414570495 FDA UDI
510(k) Number
K031560 FDA UDI
FDA Product Code
JFP FDA UDI
CGZ FDA UDI
KHP FDA UDI
JGS FDA UDI
CGA FDA UDI
GKR FDA UDI
CEM FDA UDI
CHL FDA UDI
GMDN Term
Hydrogen (H+)/pH electrode IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1145 FDA UDI
862.1170 FDA UDI
862.1450 FDA UDI
862.1665 FDA UDI
862.1345 FDA UDI
864.5620 FDA UDI
862.1600 FDA UDI
862.1120 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

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: Hydrogen (H+)/pH electrode IVD

RAPIDLab® 1200 pH Electrode Fill by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrogen (H+)/pH electrode IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 321ca3ab-a9f6-4f28-9f4d-931ffb67bc9e 37 fields · synced May 30, 2026