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Lap Scope WarmOR

FDA UDI

Class I (US FDA UDI)

by The O R Company Pty Ltd

Identity

Trade Name
Lap Scope WarmOR FDA UDI
Generic Name
Instrument warmer, electric FDA UDI
Model / Reference
SW-5-10-R FDA UDI

Identifiers

Primary DI / UDI-DI
09349967003268 FDA UDI
FDA Product Code
NWV FDA UDI
GMDN Term
Instrument warmer, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1720 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument warmer, electric

Lap Scope WarmOR by The O R Company Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument warmer, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 962d4aa8-b0a5-4095-8335-da2f71ea0769 32 fields · synced May 31, 2026