FDA UDI Not in Commercial Distribution 🇺🇸 United States

Newport

DI: 10381780004271 · Model: 62-7555 · Seaspine, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Newport
Primary DI
10381780004271
Version / Model
62-7555
Catalog Number
62-7555
Company Name
Seaspine, Inc.
Labeler DUNS
119614407
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-13
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
5637dd60-2b53-48a2-9d4e-3ee4e581b327
Distribution End Date
2017-02-13

Device Description

Cannulated Reduction Polyaxial Screw, Ø7.5 x 55mm

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
No
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
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Secondary M5566275551
Primary 10381780004271

Device Sizes

Type Value Unit Text
Device Size Text, specify Ø7.5 x 55mm