FDA UDI In Commercial Distribution 🇺🇸 United States

PLIF

DI: 10705034707488 · Model: SD389.115 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PLIF
Primary DI
10705034707488
Version / Model
SD389.115
Catalog Number
SD389115
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2022-04-26
Public Version Status
Update
Public Device Record Key
5d10b5eb-b5d3-4b8c-989e-29a19f86c76a

Device Description

PLIF SPREADER 15MM WITH THICKER SHAFT

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
44378 Bone distraction forceps

Identifiers

Type ID
Secondary H981SD3891150
Primary 10705034707488

Customer Contacts