FDA UDI Not in Commercial Distribution 🇺🇸 United States

INTERCEPTRE

DI: 03596010380920 · Model: 7208300 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
INTERCEPTRE
Primary DI
03596010380920
Version / Model
7208300
Catalog Number
7208300
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
ac53e196-c3a8-4003-9c90-90652401aaac
Distribution End Date
2019-12-11

Device Description

SCSRS HOOK INTRCPTR

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
HET LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

GMDN Terms

Code Name
38727 General-purpose surgical scissors, reusable

Identifiers

Type ID
Primary 03596010380920

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K970151 000