← Back to catalogue

INT, SlideCath

FDA UDI

Class II (US FDA UDI)

by Shanghai Kindly Medical Instruments Co., Ltd.

Identity

Trade Name
INT,SlideCath FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
5F MPB2 100cm FDA UDI
Model / Reference
ACMPB25F1100 FDA UDI
Description
5F MPB2 100cm FDA UDI

Identifiers

Primary DI / UDI-DI
06950900931888 FDA UDI
510(k) Number
K201929 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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 catheter, single-use

INT, SlideCath 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 catheter, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1f1360ed-fb40-43a3-9854-6f17f6f4a267 34 fields · synced May 30, 2026