FDA UDI In Commercial Distribution 🇺🇸 United States

SONICWELD RX, STERILE

DI: 10888118099706 · Model: 52-622-24-04 · KLS-Martin L.P.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
SONICWELD RX, STERILE
Primary DI
10888118099706
Version / Model
52-622-24-04
Company Name
KLS-Martin L.P.
Labeler DUNS
826499238
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-05-23
Public Version
5
Public Version Date
2019-08-23
Public Version Status
Update
Public Device Record Key
04b7a27b-24a9-45cf-8905-9698265de2eb

Device Description

SONICPIN RXG, PLLA-PGA

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWO Plate, cranioplasty, preformed, alterable
HBW FASTENER, PLATE, CRANIOPLASTY

GMDN Terms

Code Name
46639 Craniofacial bone tack, bioabsorbable

Identifiers

Type ID
Primary 10888118099706
Unit of Use 00888118099709

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.1 X 4 MM