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 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 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: ST014606 FDA UDI
Primary DI / UDI-DI: 00724995154974 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 751f51aa-21df-4940-afe2-fac06e78be14 36 fields · synced Jun 8, 2026