Insulated Clik Tite

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: Insulated Clik Tite FDA UDI
Generic Name: External cuff/pad connection tubing FDA UDI
Model / Reference: 8001-064-037 FDA UDI

Identifiers

Catalog Number: 8001-064-037 FDA UDI
Primary DI / UDI-DI: 07613327175295 FDA UDI
510(k) Number: K152266 FDA UDI
FDA Product Code: DWJ FDA UDI
GMDN Term: External cuff/pad connection tubing FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: External cuff/pad connection tubing

Insulated Clik Tite by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K152266 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 4268a1f5-a9ed-4aa3-b5e6-dcb7044df1b8 34 fields · synced May 30, 2026