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ORLocate

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
ORLocate FDA UDI
Generic Name
Radio-frequency identification reader FDA UDI
Device Name
ORLocate Locator Drape with two straps, non-sterile is used with the ORLocate Sponge Solution System. FDA UDI
Model / Reference
ORLocate Drape FDA UDI
Description
ORLocate Locator Drape with two straps, non-sterile is used with the ORLocate Sponge Solution System. FDA UDI

Identifiers

Catalog Number
LC16601NS FDA UDI
Primary DI / UDI-DI
10724995221659 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Radio-frequency identification reader FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Radio-frequency identification reader

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

Similar devices

Also classified as Radio-frequency identification reader.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 13f7d7e3-701e-411d-a500-08d2127953e9 35 fields · synced Jun 8, 2026