FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034721767 · Model: 03.702.223S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034721767
Version / Model
03.702.223S
Catalog Number
03702223S
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
77e3c3c6-d609-4c5f-ad53-c2a4c43f4207
Distribution End Date
2020-04-30

Device Description

BIOPSY NEEDLE KIT 10G

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
MJG DEVICE, PERCUTANEOUS, BIOPSY

GMDN Terms

Code Name
46750 Vertebral bone biopsy procedure kit, single-use

Identifiers

Type ID
Secondary H98103702223S0
Primary 10705034721767
Direct Marking 07611819371316

Customer Contacts