FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982309181 · Model: SD03.037.116 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982309181
Version / Model
SD03.037.116
Catalog Number
SD03037116
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-02
Public Version
2
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
5b7361e6-4648-47a2-be0c-fb04a55c8952

Device Description

COMPRESSION DEVICE SCREWDRIVER ACTIVATION

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47875 Bone-nailing compression screw

Identifiers

Type ID
Primary 10886982309181

Customer Contacts