FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034716152 · Model: 03.616.013 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034716152
Version / Model
03.616.013
Catalog Number
03616013
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
22f63196-2338-4ffd-9871-32b42146f379
Distribution End Date
2017-11-01

Device Description

PERSUADER

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44804 Orthopaedic rod reducer

Identifiers

Type ID
Direct Marking 07611819935662
Secondary H981036160130
Primary 10705034716152

Customer Contacts