FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886982193759 · Model: 351.23 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982193759
Version / Model
351.23
Catalog Number
35123
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
4
Public Version Date
2020-06-18
Public Version Status
Update
Public Device Record Key
550d2e7e-241e-4670-ba15-5e2efea732d9
Distribution End Date
2020-06-18

Device Description

13.0MM/3.2MM TROCAR

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47457 Orthopaedic trocar blade, reusable

Identifiers

Type ID
Secondary H6793512308
Primary 10886982193759

Customer Contacts