FDA UDI In Commercial Distribution 🇺🇸 United States

Lineum®

DI: 00888480511557 · Model: 14-525053 · ZIMMER BIOMET INC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lineum®
Primary DI
00888480511557
Version / Model
14-525053
Catalog Number
14-525053
Company Name
ZIMMER BIOMET INC
Labeler DUNS
045576443
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-07
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
2a6cdb9a-e923-41f3-a07a-c6c8d5fb2645

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
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
MNH Orthosis, spondylolisthesis spinal fixation
MNI Orthosis, spinal pedicle fixation
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MAX Intervertebral fusion device with bone graft, lumbar
MQP Spinal vertebral body replacement device

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 00888480511557

Customer Contacts