← Back to catalogue

Sensor Drive

FDA UDI

Class I (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name
SENSOR DRIVE FDA UDI
Generic Name
Operating room equipment remote control FDA UDI
Model / Reference
100969F0 FDA UDI

Identifiers

Primary DI / UDI-DI
04046768104969 FDA UDI
FDA Product Code
JEA FDA UDI
GMDN Term
Operating room equipment remote control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating room equipment remote control

Sensor Drive by Maquet, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room equipment remote control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Maquet, Inc.

Sources (1)

  • FDA UDI b956d512-5d03-4c89-b78d-4a4e7df8d128 32 fields · synced Jun 6, 2026