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Connecting Tube

FDA UDI

Class II (US FDA UDI)

by Tianck Medical Co., Ltd.

Identity

Trade Name
Connecting Tube FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Model / Reference
1200PSI 30CM FDA UDI

Identifiers

Catalog Number
043002 FDA UDI
Primary DI / UDI-DI
06971162810650 FDA UDI
FDA Product Code
BYY FDA UDI
GMDN Term
Invasive blood pressure monitoring tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

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

Yes

FDA UDI

Category: Invasive blood pressure monitoring tubing set

Connecting Tube by Tianck Medical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive blood pressure monitoring tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05a824e4-f56b-4f57-a917-cb99e627c351 33 fields · synced May 31, 2026