FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587074726 · Model: SD420.424 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587074726
Version / Model
SD420.424
Catalog Number
SD420424
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-15
Public Version
1
Public Version Date
2022-07-25
Public Version Status
New
Public Device Record Key
685013de-2638-41be-b24c-b68a812e15d4

Device Description

PSI SD420.424 TITANIUM IMPLANT

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GXN PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE

GMDN Terms

Code Name
58908 Custom-made cranial bone prosthesis

Identifiers

Type ID
Secondary H980SD42042403
Primary 10887587074726

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033868 000