Profi disposable syringe - 1. Disposable Syringe2. Intended use : To inject - Shinchang Medical Co., Ltd.

Duns Number:631088403

Device Description: 1. Disposable Syringe2. Intended use : To inject fluids into or withdraw fluids out of the 1. Disposable Syringe2. Intended use : To inject fluids into or withdraw fluids out of the body.3. Instructions for use1) Expose needle by removing needle cover.2) Inject the fluid into syringe by pulling plunger3) After injecting the injection fluid into the syringe, inject into disinfected area by pushing plunger.4) After injecting the fluid into the affected area, withdraw the syringe from needle and dispose immediately("Do not reuse")4. Warning1) This product is single use device, therefore it must be disposed after its use 2) Do not reuse after suction the medicines.3) Do not use individual packages that are opened or damaged because sterilization is not guaranteed.4) Do not use damaged or bent needle before use.5) Do not use the product when it finds foreign substances before use6) To prevent secondary contamination, open the package before use.7) Do not use the product except general injection purposes.8) Do not attempt to close the needle cover after use. If you are pierced by contaminated needle, various infections can infected5. StorageAvoid direct sunlight and store at room temperature in a dry and clean place.6. CautionFederal law restricts this device to sale by or on the order of a physician.7. Expiry Date : 3 years from manufacturing date

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More Product Details

Catalog Number

-

Brand Name

Profi disposable syringe

Version/Model Number

Profi LDS syringe 1mL 26G×1"

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FMF

Product Code Name

Syringe, Piston

Device Record Status

Public Device Record Key

e07dc5b1-3aa9-42d5-aa46-5e678c700acc

Public Version Date

May 28, 2021

Public Version Number

1

DI Record Publish Date

May 20, 2021

Additional Identifiers

Package DI Number

18800109001590

Quantity per Package

100

Contains DI Package

08800109001593

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner box