Steris

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: STERIS FDA UDI
Generic Name: Universal operating table, electromechanical FDA UDI
Device Name: The STERIS 5085 SRT Surgical Table Battery Line with Featherweight Leg Section and TLT Pads has an innovative 5th wheel design allows one caregiver to safely and easily move patients from pre-op to OR to post-op. FDA UDI
Model / Reference: 5085 SRT Surgical Table FDA UDI
Description: The STERIS 5085 SRT Surgical Table Battery Line with Featherweight Leg Section and TLT Pads has an innovative 5th wheel design allows one caregiver to safely and easily move patients from pre-op to OR to post-op. FDA UDI

Identifiers

Catalog Number: ST014207 FDA UDI
Primary DI / UDI-DI: 00724995154950 FDA UDI
510(k) Number: K090136 FDA UDI
FDA Product Code: FQO FDA UDI
GMDN Term: Universal operating table, electromechanical 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Universal operating table, electromechanical

Steris by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal operating table, electromechanical.

TS 7500 — Baxter Medical Systems GmbH + Co. KG · Class I
TS 7500 — Baxter Medical Systems GmbH + Co. KG · Class I
TS 7500 — Baxter Medical Systems GmbH + Co. KG · Class I
CORIN mobile operating table — Maquet, Inc. · Class I
TS 7500 — Baxter Medical Systems GmbH + Co. KG · Class II
Clarity — Skytron, LLC · Class I
Auxiliary base connector kit — Skytron, LLC · Class I
TS 7500 — Baxter Medical Systems GmbH + Co. KG · Class I

Cleared under the same submission

K090136 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI fb2db704-3ce1-4827-98b7-d0ffb3ee2170 36 fields · synced Jun 8, 2026