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Endo Smartcap

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
ENDO SMARTCAP FDA UDI
Generic Name
Endoscopic insufflation tubing set, single-use FDA UDI
Device Name
Disposable Tubing- for Pentax GI Endoscopes Air to CO2 Adapter FDA UDI
Model / Reference
100162 FDA UDI
Description
Disposable Tubing- for Pentax GI Endoscopes Air to CO2 Adapter FDA UDI

Identifiers

Catalog Number
100162 FDA UDI
Primary DI / UDI-DI
00677964074936 FDA UDI
510(k) Number
K093665 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Endoscopic insufflation tubing set, 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

No

FDA UDI

Single Use

No

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: Endoscopic insufflation tubing set, single-use

Endo Smartcap by Medivators Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic insufflation tubing set, 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
Medivators Inc.

Sources (1)

  • FDA UDI 7c560039-1491-4b46-ac0f-69a8b0f0d20d 36 fields · synced Jun 8, 2026