FDA UDI In Commercial Distribution 🇺🇸 United States

InCompass®

DI: 00889024401396 · Model: 2102-175 · ZIMMER SPINE, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InCompass®
Primary DI
00889024401396
Version / Model
2102-175
Catalog Number
2102-175
Company Name
ZIMMER SPINE, INC.
Labeler DUNS
787663400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
8730fe0a-e2dd-44b5-bf0b-9cf8c82bbd26

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
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00889024401396

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7.5 Millimeter