FDA UDI In Commercial Distribution 🇺🇸 United States

Santis Pre Bent Rod 5.5mmx45mm

DI: 07640159550563 · Model: 101-0045 · Lanterna Medical Technologies GmbH
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Santis Pre Bent Rod 5.5mmx45mm
Primary DI
07640159550563
Version / Model
101-0045
Company Name
Lanterna Medical Technologies GmbH
Labeler DUNS
486405637
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-03
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e0a2fc15-d7c6-457f-9199-aab3223f5903

Device Description

Santis Pre Bent Rod 5.5mmx45mm

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
MR Safe
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
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
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
Primary 07640159550563

Customer Contacts

Phone
+41712800930