FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587040394 · Model: 386.900 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587040394
Version / Model
386.900
Catalog Number
386900
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
2022-04-25
Public Version Status
Update
Public Device Record Key
601d1d58-0ed3-430c-95c1-582770409232

Device Description

ARTICULATING PLATE INTRODUCER WITH PLATE HOLDING TIP

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
64479 Surgical implant handling forceps

Identifiers

Type ID
Direct Marking 07611819755802
Secondary H9803869000
Primary 10887587040394

Customer Contacts