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Endo-Ease Vista Retrograde

FDA UDI

Class II (US FDA UDI)

by Spirus Medical, LLC

Identity

Trade Name
Endo-Ease Vista Retrograde FDA UDI
Generic Name
Endoscopic overtube, single-use FDA UDI
Device Name
Endo-Ease Endoluminal Advancement System FDA UDI
Model / Reference
EEV-200 FDA UDI
Description
Endo-Ease Endoluminal Advancement System FDA UDI

Identifiers

Catalog Number
EEV-200 FDA UDI
Primary DI / UDI-DI
00867630000202 FDA UDI
510(k) Number
K080050 FDA UDI
FDA Product Code
FED FDA UDI
GMDN Term
Endoscopic overtube, single-use 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

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

No

FDA UDI

Category: Endoscopic overtube, single-use

Endo-Ease Vista Retrograde by Spirus Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic overtube, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spirus Medical, LLC

Sources (1)

  • FDA UDI 8556b569-73f7-427a-be77-75cf1e29d80c 36 fields · synced Jun 8, 2026