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Steris

FDA UDI

Class II (US FDA UDI)

by I.C. Medical, Inc.

Identity

Trade Name
STERIS FDA UDI
Generic Name
Surgical plume evacuation system tube FDA UDI
Device Name
ICM-000-0646 STERIS ESU Shroud, Short Tip & 9 Foot Tube, Sterile FDA UDI
Model / Reference
SSESHR01 FDA UDI
Description
ICM-000-0646 STERIS ESU Shroud, Short Tip & 9 Foot Tube, Sterile FDA UDI

Identifiers

Catalog Number
SSESHR01 FDA UDI
Primary DI / UDI-DI
00817688023531 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical plume evacuation system tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Steris 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 92580509-c19c-4b0a-9bba-78078d637dec 37 fields · synced May 30, 2026