FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651792205 · Model: 79220 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
18

Basic Information

Brand Name
Halyard
Primary DI
30680651792205
Version / Model
79220
Catalog Number
79220
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
18
Record Status
Published
Publish Date
2019-10-23
Public Version
3
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
8eea63f4-80a0-4a08-b717-468743d4724e

Device Description

HALYARD BASICS* Laparotomy Drape

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
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
No

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Primary 30680651792205
Unit of Use 90680651792207

Customer Contacts