NA - RASP SIZE 12 - SYNTHES (U.S.A.) LP

Duns Number:832637081

Device Description: RASP SIZE 12

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More Product Details

Catalog Number

E511212

Brand Name

NA

Version/Model Number

E5112-12

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

-

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

-

Product Code Details

Product Code

HTR

Product Code Name

RASP

Device Record Status

Public Device Record Key

f64d977e-7be8-44db-a53a-24ba400e1a0e

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

February 20, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SYNTHES (U.S.A.) LP" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1194
2 A medical device with a moderate to high risk that requires special controls. 4171
3 A medical device with high risk that requires premarket approval 30
U Unclassified 1