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Mobile CL

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems Hsg

Identity

Trade Name
Mobile CL FDA UDI
Generic Name
Sensor holder, single-use FDA UDI
Model / Reference
989803165961 FDA UDI

Identifiers

Catalog Number
989803165961 FDA UDI
Primary DI / UDI-DI
00884838030879 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Sensor holder, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sensor holder, single-use

Mobile CL by Philips Medical Systems Hsg — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sensor holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Philips Medical Systems Hsg

Sources (1)

  • FDA UDI a9d18970-ab00-4594-91a8-a8b7e5713b07 34 fields · synced May 30, 2026