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Eleview 5mL

FDA UDI

Class II (US FDA UDI)

by Cosmo Technologies, Ltd.

Identity

Trade Name
Eleview 5mL FDA UDI
Generic Name
Submucosal lift solution FDA UDI
Device Name
5 ampoules, 5 mL each. To Facilitate endoscopic resection procedures FDA UDI
Model / Reference
9000025 FDA UDI
Description
5 ampoules, 5 mL each. To Facilitate endoscopic resection procedures FDA UDI

Identifiers

Primary DI / UDI-DI
05391530190466 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

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: Submucosal lift solution

Eleview 5mL by Cosmo Technologies, Ltd. — 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
Cosmo Technologies, Ltd.

Sources (1)

  • FDA UDI 40172fcf-2cc3-45c9-813a-94795d898bfa 34 fields · synced Jun 8, 2026