FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046955206759 · Model: PV011 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046955206759
Version / Model
PV011
Catalog Number
PV011
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-29
Public Version
4
Public Version Date
2023-08-28
Public Version Status
Update
Public Device Record Key
5d9a4b07-6c1c-4c8d-b2f3-130a03874095

Device Description

UPGRADE KIT F/INTEGRATION OF 3D MONITOR

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSO MICROSCOPE, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
62379 Surgical instrument assist arm system, manually-adjusted

Identifiers

Type ID
Primary 04046955206759

Customer Contacts