FDA UDI In Commercial Distribution 🇺🇸 United States

Erisma®-LP

DI: 03700780618521 · Model: 18178530 · CLARIANCE
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Erisma®-LP
Primary DI
03700780618521
Version / Model
18178530
Catalog Number
18178530
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9a9a39e3-6720-4ea5-9a67-47849b587a2c

Device Description

POLYAXIAL REDUCTION SCREW

Device Characteristics

Single Use
Yes
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
Yes
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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 03700780618521

Customer Contacts

Phone
7738687041

Premarket Submissions

Submission Number Supplement Number
K153326 000

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Outer Diameter 8.5 Millimeter