FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653064663 · Model: BA720R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653064663
Version / Model
BA720R
Catalog Number
BA720R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
1
Public Version Date
2020-04-28
Public Version Status
New
Public Device Record Key
5c4da475-833b-431e-8c3c-34a0123562d3

Device Description

Skin graft mesher

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
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
FZW EXPANDER, SURGICAL, SKIN GRAFT

GMDN Terms

Code Name
13614 Skin graft mesher

Identifiers

Type ID
Primary 04038653064663

Customer Contacts