FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046955741731 · Model: FK097NB · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AESCULAP
Primary DI
04046955741731
Version / Model
FK097NB
Catalog Number
FK097NB
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-17
Public Version
1
Public Version Date
2025-08-25
Public Version Status
New
Public Device Record Key
d484b93f-0759-43a2-b0e4-fa820b64145a

Device Description

SQ KERRISON 10X3MM 90DG DWN STD 200MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
HAE RONGEUR, MANUAL

GMDN Terms

Code Name
64337 Bone-coring punch, reusable

Identifiers

Type ID
Primary 04046955741731

Customer Contacts