FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653281893 · Model: FF737R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653281893
Version / Model
FF737R
Catalog Number
FF737R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-19
Public Version
3
Public Version Date
2021-10-19
Public Version Status
Update
Public Device Record Key
a6e49b8a-e8b1-45e2-b0f2-ebb45baccabe

Device Description

KERRISON Bone Punch conventional, 130 °, upwards cutting, 7 7/8", (200 mm), width: 2 mm, opening width: 9 mm, not detachable, without ejector, standard, non-sterile, reusable, to be used with: JF120R

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
LRY PUNCH, SURGICAL

GMDN Terms

Code Name
64337 Bone-coring punch, reusable

Identifiers

Type ID
Primary 04038653281893

Customer Contacts