FDA UDI In Commercial Distribution 🇺🇸 United States

PULSE

DI: 10705034369907 · Model: 410270354 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSE
Primary DI
10705034369907
Version / Model
410270354
Catalog Number
410270354
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
3
Public Version Date
2018-06-26
Public Version Status
Update
Public Device Record Key
7e8fad8d-23a2-4b27-9b71-041f86adfd1c

Device Description

PULSE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL SIZING TEMPLATE 54/57mm

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
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 10705034369907

Customer Contacts