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Balloon Catheter Syringe Pump

FDA UDIEUDAMED

Class II (US FDA UDI)

by Shanghai Kinetic Medical Co., Ltd.

Identity

Trade Name
Balloon Catheter Syringe Pump FDA UDI
Generic Name
Catheter/overtube balloon inflator, single-use FDA UDI
Device Name
Balloon Catheter Syringe Pump, Tube Length 60cm FDA UDI
Model / Reference
FG4013 FDA UDI
Description
Balloon Catheter Syringe Pump, Tube Length 60cm FDA UDI

Identifiers

Catalog Number
FG4013 FDA UDI
Primary DI / UDI-DI
06938695537782 FDA UDI
510(k) Number
K113742 FDA UDI
FDA Product Code
NDN FDA UDI
HRX FDA UDI
GMDN Term
Catheter/overtube balloon inflator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3027 FDA UDI
888.1100 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

Yes

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

Dimensions & Sizes

Size
Length — 60 Centimeter FDA UDI

Category: Catheter/overtube balloon inflator, single-use

Balloon Catheter Syringe Pump by Shanghai Kinetic Medical Co., Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Catheter/overtube balloon inflator, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 7e9cd2c6-aa41-4844-a684-4619e8e31667 37 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026