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Int

FDA UDI

Class II (US FDA UDI)

by Shanghai Kindly Medical Instruments Co., Ltd.

Identity

Trade Name
INT FDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
6ml, fixed adapter; FDA UDI
Model / Reference
AS0602 FDA UDI
Description
6ml, fixed adapter; FDA UDI

Identifiers

Primary DI / UDI-DI
06950900920370 FDA UDI
510(k) Number
K170025 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiographic syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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: Angiographic syringe

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

Similar devices

Also classified as Angiographic syringe.

Cleared under the same submission

K170025 also covers:

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 8f8ae4e5-6c23-4479-bc64-9f2c5bc5f557 34 fields · synced Jun 8, 2026