FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 03596010101372 · Model: 2046 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010101372
Version / Model
2046
Catalog Number
2046
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
f6fce6f2-b464-4684-b1c9-5db667246fc9
Distribution End Date
2022-03-17

Device Description

MTO LAMP DNF TUNGSTEN/HALOGEN

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EOB NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

GMDN Terms

Code Name
35158 Endoscopic light source unit, line-powered

Identifiers

Type ID
Primary 03596010101372

Customer Contacts