AESCULAP - , non-sterile, reusable - AESCULAP, INC.

Duns Number:082594540

Device Description: , non-sterile, reusable

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More Product Details

Catalog Number

MG255R

Brand Name

AESCULAP

Version/Model Number

MG255R

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

HDQ

Product Code Name

DILATOR, CERVICAL, FIXED SIZE

Device Record Status

Public Device Record Key

0977cd95-1382-489d-957b-a4cab8c0f7b4

Public Version Date

September 02, 2020

Public Version Number

1

DI Record Publish Date

August 25, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AESCULAP, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3239
2 A medical device with a moderate to high risk that requires special controls. 683