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Radial artery closure band

FDA UDI

Class I (US FDA UDI)

by Tianck Medical Co., Ltd.

Identity

Trade Name
Radial artery closure band FDA UDI
Generic Name
Radial artery compression device FDA UDI
Model / Reference
TB-02 FDA UDI

Identifiers

Catalog Number
191002 FDA UDI
Primary DI / UDI-DI
06971162810988 FDA UDI
FDA Product Code
KCY FDA UDI
GMDN Term
Radial artery compression device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 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: Radial artery compression device

Radial artery closure band by Tianck Medical Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radial artery compression device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7aca0ac3-e6e4-47b0-974b-5a41913c90af 33 fields · synced May 30, 2026