FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034775593 · Model: 389.393 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034775593
Version / Model
389.393
Catalog Number
389393
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
2020-07-01
Public Version Status
Update
Public Device Record Key
90fb7b45-0056-46be-b268-d17d9c9d48fe
Distribution End Date
2020-07-01

Device Description

BONE CURETTE - ANGLED HEAD 5.5MM X 8.25MM/250MM LENGTH

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Direct Marking 07611819093799
Secondary H9813893930
Primary 10705034775593

Customer Contacts