FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886982235992 · Model: 485.327S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982235992
Version / Model
485.327S
Catalog Number
485327S
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
2015-09-14
Public Version
6
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
6a52a6be-23e6-48d9-97d5-2a572b742008
Distribution End Date
2019-07-06

Device Description

13MM TI CANNULATED TIBIAL NAIL 270MM - STERILE

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JDS NAIL, FIXATION, BONE

GMDN Terms

Code Name
38152 Tibia nail

Identifiers

Type ID
Secondary H679485327S0
Primary 10886982235992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K962047 000