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INT or KDL

FDA UDI

Class II (US FDA UDI)

by Shanghai Kindly Medical Instruments Co., Ltd.

Identity

Trade Name
INT or KDL FDA UDI
Generic Name
Interventional radiology percutaneous-access kit, single-use FDA UDI
Device Name
Interventional radiology percutaneous-access procedure kit. FDA UDI
Model / Reference
NIS03A FDA UDI
Description
Interventional radiology percutaneous-access procedure kit. FDA UDI

Identifiers

Primary DI / UDI-DI
06950900922305 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Interventional radiology percutaneous-access kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Interventional radiology percutaneous-access kit, single-use

INT or KDL by Shanghai Kindly Medical Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interventional radiology percutaneous-access kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shanghai Kindly Medical Instruments Co., Ltd.

Sources (1)

  • FDA UDI 41c55db4-3c14-4e27-8e87-7b85665eca5f 33 fields · synced Jun 8, 2026