FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963620486 · Model: EK238SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

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Basic Information

Brand Name
AESCULAP
Primary DI
04046963620486
Version / Model
EK238SU
Catalog Number
EK238SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2017-02-26
Public Version
8
Public Version Date
2022-01-19
Public Version Status
Update
Public Device Record Key
c2538035-053b-4b48-a08d-4d3656a911fc
Distribution End Date
2021-05-17

Device Description

DISP.TROCAR W.DILATING PIN 12/150MM

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 04046963620486
Unit of Use 04046963436322

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter (mm) : 12.000 MM
Device Size Text, specify Working length (mm) : 150.000 MM