FDA UDI In Commercial Distribution 🇺🇸 United States

INTELIJET

DI: 03596010250353 · Model: 7204811 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTELIJET
Primary DI
03596010250353
Version / Model
7204811
Catalog Number
7204811
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-23
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
6b98d914-3f36-43d5-9c41-70f697b7be67

Device Description

OBTURATOR, CONICAL TIP, FITS ALL 6.0 MM DIAGNOSTIC CANNULAS

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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 03596010250353

Customer Contacts