FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651926705 · Model: 92670 · Avanos Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10680651926705
Version / Model
92670
Catalog Number
60415
Company Name
Avanos Medical, Inc.
Labeler DUNS
079375431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-06
Public Version
3
Public Version Date
2018-11-16
Public Version Status
Update
Public Device Record Key
fdb38892-7f88-4b39-b3a0-6603b89fc412

Device Description

HALYARD* Polypectomy Snare

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FDI SNARE, FLEXIBLE

GMDN Terms

Code Name
35622 Flexible polypectomy snare, single-use

Identifiers

Type ID
Package 30680651926709
Primary 10680651926705

Customer Contacts