FDA UDI In Commercial Distribution 🇺🇸 United States

Posterior Disc Prep

DI: 10889981154301 · Model: 06-70-0207 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Posterior Disc Prep
Primary DI
10889981154301
Version / Model
06-70-0207
Catalog Number
06-70-0207
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-21
Public Version
1
Public Version Date
2018-08-21
Public Version Status
New
Public Device Record Key
93d98512-adbd-4062-b01c-a5a93c51e6d5

Device Description

Paddle Distractor, 7mm

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
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 10889981154301

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 7mm