FDA UDI In Commercial Distribution 🇺🇸 United States

Kerrison

DI: 04049197515115 · Model: 259-401-360 · RZ-Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kerrison
Primary DI
04049197515115
Version / Model
259-401-360
Company Name
RZ-Medizintechnik GmbH
Labeler DUNS
312953227
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-02
Public Version
1
Public Version Date
2023-05-10
Public Version Status
New
Public Device Record Key
ad052806-3a8c-47f2-b0f1-e9607c7baff8

Device Description

Kerrison, 4.0 x 360mm, 90°

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
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 04049197515115