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LapPakOR

FDA UDI

Class I (US FDA UDI)

by The O R Company Pty Ltd

Identity

Trade Name
LapPakOR FDA UDI
Generic Name
Viscera retention paddle FDA UDI
Device Name
Single piece bowel retractor FDA UDI
Model / Reference
W-18 FDA UDI
Description
Single piece bowel retractor FDA UDI

Identifiers

Catalog Number
W-18 FDA UDI
Primary DI / UDI-DI
09349967000700 FDA UDI
FDA Product Code
GCZ FDA UDI
GMDN Term
Viscera retention paddle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Viscera retention paddle

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

Similar devices

Also classified as Viscera retention paddle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7a2506bc-1f69-45c3-bfa1-8c54f95913db 34 fields · synced Jun 1, 2026