FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20887587030477 · Model: 304.123 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20887587030477
Version / Model
304.123
Catalog Number
304123
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-12-31
Public Version
3
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
21902327-ac16-4ad9-bbe4-83c7ad79a9b5

Device Description

SCREW LENGTH MARKER-23MM

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
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Secondary H9803041230
Primary 20887587030477
Unit of Use 80887587030479

Customer Contacts