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Gbuk

FDA UDI

Class II (US FDA UDI)

by Jiangsu Caina Medical Co., Ltd

Identity

Trade Name
GBUK FDA UDI
Generic Name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI
Device Name
3 ml SP Prefilled saline syringe 0.9%Sodium Chloride(0.9%Na Cl),USP FDA UDI
Model / Reference
3mL FDA UDI
Description
3 ml SP Prefilled saline syringe 0.9%Sodium Chloride(0.9%Na Cl),USP FDA UDI

Identifiers

Catalog Number
PFS-3SSU FDA UDI
Primary DI / UDI-DI
06971564461115 FDA UDI
510(k) Number
K220060 FDA UDI
FDA Product Code
NGT FDA UDI
GMDN Term
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Category: Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

Gbuk by Jiangsu Caina Medical Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 145e2b19-a7f1-4dbd-ad83-8393f3b5fa2b 35 fields · synced May 30, 2026