FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963892890 · Model: BA716SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
AESCULAP
Primary DI
04046963892890
Version / Model
BA716SU
Catalog Number
BA716SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-04-24
Public Version
3
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
9f9fdc6c-3847-44f8-b055-6ea307a667a2

Device Description

Dermatome Spare Blade (43 mm), sterile, package of 10 pieces

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
GFD Dermatome

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Unit of Use 04046963835811
Primary 04046963892890

Customer Contacts