FDA UDI In Commercial Distribution 🇺🇸 United States

ACF

DI: 10705034709246 · Model: SD396.933 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ACF
Primary DI
10705034709246
Version / Model
SD396.933
Catalog Number
SD396933
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
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
61e81b20-92ca-45a2-b6a8-393a84a8e5ef

Device Description

ACF STICK TRIAL RASP BIPLANAR STOPS/LORDOTIC/7MM

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
HTR RASP

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Secondary H981SD3969330
Primary 10705034709246

Customer Contacts