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RenovaRP

FDA UDI

Class II (US FDA UDI)

by GI Supply, Inc.

Identity

Trade Name
RenovaRP FDA UDI
Generic Name
Pleurocentesis/paracentesis kit FDA UDI
Device Name
RenovaRP Fluid Drainage Bag to be used with RenovaRP Centesis Pump - sold in box of 20 FDA UDI
Model / Reference
GIS-29 FDA UDI
Description
RenovaRP Fluid Drainage Bag to be used with RenovaRP Centesis Pump - sold in box of 20 FDA UDI

Identifiers

Catalog Number
GIS-29 FDA UDI
Primary DI / UDI-DI
00893029002151 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Pleurocentesis/paracentesis kit 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pleurocentesis/paracentesis kit

RenovaRP by GI Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleurocentesis/paracentesis kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GI Supply, Inc.

Sources (1)

  • FDA UDI 5df67407-7675-4c3c-8a7c-3060a5f240af 35 fields · synced May 30, 2026