FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03663136010571 · Model: PL1-A003-13 · SPINEVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03663136010571
Version / Model
PL1-A003-13
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-01
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
9f769d28-7c81-4d54-a2da-31872823dd3d

Device Description

Reamer 13

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
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
HTO Reamer

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 03663136010571

Customer Contacts

Phone
+33153332525

Device Sizes

Type Value Unit Text
Width 13 Millimeter
Length 283 Millimeter