FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034732671 · Model: 03.841.411 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034732671
Version / Model
03.841.411
Catalog Number
03841411
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
4
Public Version Date
2022-04-26
Public Version Status
Update
Public Device Record Key
e465d244-b7cc-4867-9177-adab0afe0c51

Device Description

DOUBLE-SIDED TRIAL SPACER PARALLEL/LRG 11MM/12MM HEIGHT

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
HWT TEMPLATE

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Direct Marking 07611819473539
Secondary H981038414110
Primary 10705034732671

Customer Contacts