AESCULAP - ADTEC MINI Dissecting Forceps, complete - Aesculap AG

Duns Number:315018218

Device Description: ADTEC MINI Dissecting Forceps, complete instrument, straight, (200 mm), diam. 3,50 mm, dou ADTEC MINI Dissecting Forceps, complete instrument, straight, (200 mm), diam. 3,50 mm, double action, consisting of PM987P, PO364R,PO380R, reusable

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More Product Details

Catalog Number

PO324R

Brand Name

AESCULAP

Version/Model Number

PO324R

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

GEI

Product Code Name

ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Device Record Status

Public Device Record Key

89acb5d1-ed65-4b30-9299-1bfa245dd330

Public Version Date

October 27, 2021

Public Version Number

4

DI Record Publish Date

September 23, 2016

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