FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651487835 · Model: 48783 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
11

Basic Information

Brand Name
Halyard
Primary DI
30680651487835
Version / Model
48783
Catalog Number
48783NS
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
11
Record Status
Published
Publish Date
2022-02-17
Public Version
1
Public Version Date
2022-02-25
Public Version Status
New
Public Device Record Key
0e41ca34-0408-46ab-a4ff-8b57b49fb289

Device Description

Femoral Angiography with Pouch, 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
Yes
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
Unit of Use 90680651487837
Primary 30680651487835

Customer Contacts