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BOA Endoscopic Valve

FDA UDI

Class II (US FDA UDI)

by C2 Therapeutics, Inc.

Identity

Trade Name
BOA Endoscopic Valve FDA UDI
Generic Name
Endoscope assembly adaptor FDA UDI
Device Name
BOA Endoscopic Valve, Endoscopic Accessory FDA UDI
Model / Reference
FG-1016 FDA UDI
Description
BOA Endoscopic Valve, Endoscopic Accessory FDA UDI

Identifiers

Catalog Number
FG-1016 FDA UDI
Primary DI / UDI-DI
00854924006163 FDA UDI
510(k) Number
K152140 FDA UDI
FDA Product Code
OCX FDA UDI
GMDN Term
Endoscope assembly adaptor 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

No

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: Endoscope assembly adaptor

BOA Endoscopic Valve by C2 Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope assembly adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 833f1e22-2974-4508-a099-0b95779b95e1 35 fields · synced May 30, 2026