FDA UDI In Commercial Distribution 🇺🇸 United States

VIPER

DI: 10705034282909 · Model: 186727950 · Medos International Sàrl
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VIPER
Primary DI
10705034282909
Version / Model
186727950
Catalog Number
186727950
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-02
Public Version
5
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
001c4376-430a-4407-8c85-3bd2241750c9

Device Description

VIPER SYSTEM FENESTRATED CORTICAL FIX POLYAXIAL SCREW 5.5 x 9 x 50mm

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
PML bone cement, posterior screw augmentation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 10705034282909

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160879 000