FDA UDI In Commercial Distribution 🇺🇸 United States

HERMES

DI: 03596010493736 · Model: 7210017 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HERMES
Primary DI
03596010493736
Version / Model
7210017
Catalog Number
7210017
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
e8016712-a5bf-43b7-9653-e013a27a27ee

Device Description

INTERFACE KIT HERMES TO S&N 400 INSUF

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
48169 Insufflation gas conditioning system control unit

Identifiers

Type ID
Primary 03596010493736

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K050580 000