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Altrix Temperature Management Hose

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Altrix Temperature Management Hose FDA UDI
Generic Name
External cuff/pad connection tubing FDA UDI
Model / Reference
8003-002-107 FDA UDI

Identifiers

Catalog Number
8003-002-107 FDA UDI
Primary DI / UDI-DI
07613327369014 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External cuff/pad connection tubing

Altrix Temperature Management Hose by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External cuff/pad connection tubing.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI bbf246ff-3169-4b4d-9df3-a1055417229b 34 fields · synced May 31, 2026