FDA UDI In Commercial Distribution 🇺🇸 United States

ACCS

DI: 10705034768151 · Model: 304.972 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ACCS
Primary DI
10705034768151
Version / Model
304.972
Catalog Number
304972
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
2016-12-31
Public Version
8
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
a08f2864-3040-4d3c-bc4f-4d8d1b3ab317

Device Description

MODULE F/1&2 LEVEL TI ANTERIOR CERV COMPRESSION SYS PLATES

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Secondary H9813049720
Primary 10705034768151

Customer Contacts