FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034732220 · Model: 03.841.025 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034732220
Version / Model
03.841.025
Catalog Number
03841025
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
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
7ddae3a5-5d95-4873-aa52-d10dcd129d23

Device Description

TRIAL RASP-LORDOTIC 5MM 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
HTR RASP

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Direct Marking 07611819530027
Secondary H981038410250
Primary 10705034732220

Customer Contacts