FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963620172 · Model: EK124SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AESCULAP
Primary DI
04046963620172
Version / Model
EK124SU
Catalog Number
EK124SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2017-02-26
Public Version
9
Public Version Date
2020-07-01
Public Version Status
Update
Public Device Record Key
03668b0f-154b-4131-89a6-a5165dd84398

Device Description

DISP.TROCAR SLEEVE 10/110MM SMOOTH W.TAP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
42412 Laparoscopic access cannula, single-use

Identifiers

Type ID
Primary 04046963620172
Unit of Use 04046963426361

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Working length (mm) : 110.000 MM
Device Size Text, specify Diameter (mm) : 10.000 MM