FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034728308 · Model: 03.815.075 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034728308
Version / Model
03.815.075
Catalog Number
03815075
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
2
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
1cfcedf2-b91f-42ea-9702-06be052d9318

Device Description

EVOLUTION PUSH BLOCK-RECESSED 6MM

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44378 Bone distraction forceps

Identifiers

Type ID
Direct Marking 07611819534568
Secondary H981038150750
Primary 10705034728308

Customer Contacts