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ESU Sensor

FDA UDI

Class II (US FDA UDI)

by I.C. Medical, Inc.

Identity

Trade Name
ESU Sensor FDA UDI
Generic Name
Surgical plume evacuation system FDA UDI
Model / Reference
2250 FDA UDI

Identifiers

Catalog Number
ICM-000-0422 FDA UDI
Primary DI / UDI-DI
00817688021742 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Surgical plume evacuation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5070 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

ESU Sensor by I.C. Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.C. Medical, Inc.

Sources (1)

  • FDA UDI e5733fc6-c678-4582-a38f-9cf7d4e4d655 34 fields · synced May 30, 2026