FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04041906505608 · Model: FX008SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
AESCULAP
Primary DI
04041906505608
Version / Model
FX008SU
Catalog Number
FX008SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2023-04-03
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
88bf5a01-87b3-4c52-bb45-e4c189f5e602

Device Description

TUNNELLER 700MM STANDARD

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
Yes
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
GYK Instrument, shunt system implantation

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Unit of Use 04041906507404
Primary 04041906505608

Customer Contacts