RELI® - REDILON PRO BLK MF 4-0 YFS-2 10" - MYCO MEDICAL SUPPLIES INC.

Duns Number:879187821

Device Description: REDILON PRO BLK MF 4-0 YFS-2 10"

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More Product Details

Catalog Number

N6621-M

Brand Name

RELI®

Version/Model Number

N6621-M

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K172149,K172149,K172149

Product Code Details

Product Code

GAR

Product Code Name

Suture, Nonabsorbable, Synthetic, Polyamide

Device Record Status

Public Device Record Key

99d406e4-3764-4347-bd31-06ec17cba983

Public Version Date

September 23, 2021

Public Version Number

1

DI Record Publish Date

September 15, 2021

Additional Identifiers

Package DI Number

10386120011742

Quantity per Package

12

Contains DI Package

00386120011745

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Carton

"MYCO MEDICAL SUPPLIES INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7
2 A medical device with a moderate to high risk that requires special controls. 471