FDA UDI In Commercial Distribution 🇺🇸 United States

L-Varlock

DI: 00850011324103 · Model: 103 · SPINESOURCE INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
L-Varlock
Primary DI
00850011324103
Version / Model
103
Catalog Number
HA-002
Company Name
SPINESOURCE INC
Labeler DUNS
150955560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-11
Public Version
1
Public Version Date
2019-10-21
Public Version Status
New
Public Device Record Key
7dca3213-09b1-43e7-8e27-c1618d2dc8a7

Device Description

Instrument, Slap Hammer Adapter

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
47814 Orthopaedic implantation hammering attachment

Identifiers

Type ID
Primary 00850011324103