FDA UDI In Commercial Distribution 🇺🇸 United States

KINCISE

DI: 10886982348111 · Model: 2000-00-101 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KINCISE
Primary DI
10886982348111
Version / Model
2000-00-101
Catalog Number
200000101
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-31
Public Version
1
Public Version Date
2024-11-08
Public Version Status
New
Public Device Record Key
ee3b86e4-684b-4e4c-9cca-4246814ccaf6

Device Description

KINCISE(TM) SYSTEM SURGICAL HANDPIECE CASE

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
No

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Direct Marking 07612334260079
Primary 10886982348111

Customer Contacts