FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587078137 · Model: 60.501.127 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
10887587078137
Version / Model
60.501.127
Catalog Number
60501127
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-21
Public Version
1
Public Version Date
2024-08-29
Public Version Status
New
Public Device Record Key
eae142d1-5c7f-48ae-bd0e-5b87184939d9

Device Description

MATRIXSTERNUM INSTRUMENT TRAY

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
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
HWC Screw, fixation, bone
HRS Plate, fixation, bone

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Direct Marking 07612334263520
Primary 10887587078137

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233967 000