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LiftUp

FDA UDI

Class II (US FDA UDI)

by Ovesco Endoscopy AG

Identity

Trade Name
LiftUp FDA UDI
Generic Name
Submucosal lift solution FDA UDI
Device Name
LiftUp is a thermoreversible injection agent for endoscopic mucosal resection (EMR) and/or endoscopic submucosal dissection (ESD) FDA UDI
Model / Reference
LiftUp FDA UDI
Description
LiftUp is a thermoreversible injection agent for endoscopic mucosal resection (EMR) and/or endoscopic submucosal dissection (ESD) FDA UDI

Identifiers

Catalog Number
200.56.01 FDA UDI
Primary DI / UDI-DI
04260206311003 FDA UDI
FDA Product Code
PLL FDA UDI
GMDN Term
Submucosal lift solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Category: Submucosal lift solution

LiftUp by Ovesco Endoscopy AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Submucosal lift solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ovesco Endoscopy AG

Sources (1)

  • FDA UDI a8dcd881-fdfb-4c19-a710-8c295dc08646 36 fields · synced Jun 8, 2026