FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653045983 · Model: FK723R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653045983
Version / Model
FK723R
Catalog Number
FK723R
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
546690ed-e88f-41fb-88e2-5e101b3b459d

Device Description

BUSHE Bone Curette, angled downwards, 9 3/4", (250 mm), width: 3 mm, non-sterile, reusable

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
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
FZS CURETTE, SURGICAL, GENERAL USE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 04038653045983

Customer Contacts