FDA UDI In Commercial Distribution 🇺🇸 United States

PULSE

DI: 10705034369624 · Model: 410210200 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSE
Primary DI
10705034369624
Version / Model
410210200
Catalog Number
410210200
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
18debb1d-e835-4f44-a52e-ad573413fad8

Device Description

PULSE ANTERIOR CERVICAL PLATE SYSTEM SCREW STARTER

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
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
32859 Orthopaedic bone screw starter/notcher

Identifiers

Type ID
Primary 10705034369624

Customer Contacts