FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982005748 · Model: SD357.013 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982005748
Version / Model
SD357.013
Catalog Number
SD357013
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
3
Public Version Date
2022-04-28
Public Version Status
Update
Public Device Record Key
89527dd4-e8a3-4d77-9190-44f915c20d65

Device Description

COMPRESSION DEVICE FOR RETRO/ANTEGRADE FEM NAIL-EX

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
HWN INSTRUMENT, COMPRESSION

GMDN Terms

Code Name
47875 Bone-nailing compression screw

Identifiers

Type ID
Secondary H679SD3570130
Primary 10886982005748

Customer Contacts