IMEDICOM SAW BLADE - IMEDICOM CO., LTD.

Duns Number:690340653

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More Product Details

Catalog Number

-

Brand Name

IMEDICOM SAW BLADE

Version/Model Number

PSN-110B

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

GFA

Product Code Name

Blade, Saw, General & Plastic Surgery, Surgical

Device Record Status

Public Device Record Key

56297a39-128e-43e3-bf20-c051b23e5c0e

Public Version Date

January 22, 2021

Public Version Number

3

DI Record Publish Date

July 13, 2018

Additional Identifiers

Package DI Number

08800038021761

Quantity per Package

10

Contains DI Package

08809317178653

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"IMEDICOM CO., LTD." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2527
2 A medical device with a moderate to high risk that requires special controls. 59