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JosNoe Medical Inc

FDA UDI

Class I (US FDA UDI)

by JosNoe Medical Inc

Identity

Trade Name
JosNoe Medical Inc FDA UDI
Generic Name
Endoscopic insufflation tubing set, single-use FDA UDI
Device Name
Insufflation Tubing Set with Filter, Quick Connector and Luer Lock FDA UDI
Model / Reference
SP-102 FDA UDI
Description
Insufflation Tubing Set with Filter, Quick Connector and Luer Lock FDA UDI

Identifiers

Primary DI / UDI-DI
00850003294308 FDA UDI
FDA Product Code
NKC FDA UDI
GMDN Term
Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1730 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

Yes

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

JosNoe Medical Inc by JosNoe Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic insufflation tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
JosNoe Medical Inc

Sources (1)

  • FDA UDI 9fe8378f-29ce-4842-8015-95cd3dcc85cb 33 fields · synced May 30, 2026