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Click-Tip

FDA UDI

Class II (US FDA UDI)

by Medi-Globe Corporation

Identity

Trade Name
Click-Tip FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Device Name
Click-Tip Injection Needle, 19 G, Needle Length 4 mm, Catheter Diameter 2.3 mm, Sheath Length 230 cm FDA UDI
Model / Reference
02-23-230 FDA UDI
Description
Click-Tip Injection Needle, 19 G, Needle Length 4 mm, Catheter Diameter 2.3 mm, Sheath Length 230 cm FDA UDI

Identifiers

Catalog Number
02-23-230 FDA UDI
Primary DI / UDI-DI
04052838015523 FDA UDI
FDA Product Code
FBK FDA UDI
GMDN Term
General-purpose endoscopic needle, 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: General-purpose endoscopic needle, single-use

Click-Tip by Medi-Globe Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose endoscopic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb78510f-b1fe-4568-af9b-87ffbd0fdc8c 36 fields · synced May 30, 2026