FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034721736 · Model: 03.702.220S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034721736
Version / Model
03.702.220S
Catalog Number
03702220S
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2020-05-01
Public Version Status
Update
Public Device Record Key
b4bf2c4d-9f38-42e1-802b-35331393d2d7
Distribution End Date
2020-04-30

Device Description

VERTEBROPLASTY NEEDLE KIT 12G DIAMOND TIP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
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
KIH DISPENSER, CEMENT

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Secondary H98103702220S0
Primary 10705034721736
Direct Marking 07611819371286

Customer Contacts