FDA UDI Not in Commercial Distribution 🇺🇸 United States

Stainless Steel

DI: 10381780023340 · Model: SSDF2FXIMP · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Stainless Steel
Primary DI
10381780023340
Version / Model
SSDF2FXIMP
Catalog Number
SSDF2FXIMP
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
bb66ce8f-6c83-4935-8a00-ecd3a83ae010
Distribution End Date
2015-11-15

Device Description

Fixed Screws 6.35mm SS Sterilization Case Assembly

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

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

Identifiers

Type ID
Secondary M248SSDF2FXIMP1
Primary 10381780023340

Customer Contacts