FDA UDI Not in Commercial Distribution 🇺🇸 United States

INTERCEPTRE

DI: 03596010380814 · Model: 7207300 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTERCEPTRE
Primary DI
03596010380814
Version / Model
7207300
Catalog Number
7207300
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
9
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0a4be446-5ed9-48cb-a17d-a06d8ef6f8d8
Distribution End Date
2017-03-28

Device Description

TRAY INSERT INTRCPTR INST.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 03596010380814

Customer Contacts