FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034772783 · Model: 388.398 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034772783
Version / Model
388.398
Catalog Number
388398
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
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
04156215-0e7e-4051-b03b-ccf5f5b55e66
Distribution End Date
2020-09-17

Device Description

2.5MM HEXAGONAL SCREWDRIVER W/THREADED HOLDING SLEEVE

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
HXX SCREWDRIVER

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Direct Marking 07611819795297
Secondary H9813883980
Primary 10705034772783

Customer Contacts