FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04041906131982 · Model: FV003R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
AESCULAP
Primary DI
04041906131982
Version / Model
FV003R
Catalog Number
FV003R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-06-23
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
6304c9a6-f499-4c50-bd0e-bdb3f715336e

Device Description

TUNNELING INSTRUMENT 450MM

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
HAO INSTRUMENT, SURGICAL, NON-POWERED

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Primary 04041906131982
Unit of Use 04038653342617

Customer Contacts