FDA UDI In Commercial Distribution 🇺🇸 United States

Navio

DI: 20885556628724 · Model: PFSD01009 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
Navio
Primary DI
20885556628724
Version / Model
PFSD01009
Catalog Number
PFSD01009
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2016-01-22
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
60120e7a-d2af-4c5e-9a89-c6d2f4a9ea19

Device Description

Navio Checkpoint Verification Pins

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
No
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
OLO Orthopedic stereotaxic instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 20885556628724
Unit of Use 00885556628720

Customer Contacts