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Orca®

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Orca® FDA UDI
Generic Name
Endoscope air/water valve, single-use FDA UDI
Device Name
Single Use Air/Water and Suction Valves FDA UDI
Model / Reference
SUV-618-01 FDA UDI
Description
Single Use Air/Water and Suction Valves FDA UDI

Identifiers

Catalog Number
SUV-618-01 FDA UDI
Primary DI / UDI-DI
08714729993728 FDA UDI
FDA Product Code
ODC FDA UDI
GMDN Term
Endoscope air/water valve, 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

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

No

FDA UDI

Category: Endoscope suction valve, single-useEndoscope air/water valve, single-use

Orca® by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope air/water valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 61e9cc82-8814-4899-b600-d8bf63d5e036 34 fields · synced May 30, 2026