FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00885554021219 · Model: 72203120 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885554021219
Version / Model
72203120
Catalog Number
72203120
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
73d3aad0-da7b-4c7c-9260-5ba554bd99e7
Distribution End Date
2020-08-04

Device Description

2.7MM DIAMETER GUIDE PIN

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
Yes
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
No

Product Codes

Code Name
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
47900 Orthopaedic implant calibration pin

Identifiers

Type ID
Primary 00885554021219

Customer Contacts