FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034721941 · Model: 03.702.751S · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034721941
Version / Model
03.702.751S
Catalog Number
03702751S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-31
Public Version
2
Public Version Date
2022-04-26
Public Version Status
Update
Public Device Record Key
7621393c-9993-4e89-b198-fdf785b0706c

Device Description

CAVITY CREATION INSTRUMENT 15MM-STERILE

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCJ spinal channeling instrument, vertebroplasty

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Secondary H98103702751S0
Primary 10705034721941

Customer Contacts