AESCULAP - TUEBINGEN Vaginal Retractor, 10 1/2", (265 mm), - Aesculap AG

Duns Number:315018218

Device Description: TUEBINGEN Vaginal Retractor, 10 1/2", (265 mm), depth: 95 mm, width: 20 mm, non-sterile, r TUEBINGEN Vaginal Retractor, 10 1/2", (265 mm), depth: 95 mm, width: 20 mm, non-sterile, reusable

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More Product Details

Catalog Number

EL868R

Brand Name

AESCULAP

Version/Model Number

EL868R

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

HDL

Product Code Name

RETRACTOR, VAGINAL

Device Record Status

Public Device Record Key

b68575cc-0d96-4711-927a-7c68441f150e

Public Version Date

April 29, 2020

Public Version Number

1

DI Record Publish Date

April 21, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AESCULAP AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 11840
2 A medical device with a moderate to high risk that requires special controls. 7088
3 A medical device with high risk that requires premarket approval 37