FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651490446 · Model: 49044 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Halyard
Primary DI
30680651490446
Version / Model
49044
Catalog Number
49044
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2023-08-17
Public Version
1
Public Version Date
2023-08-25
Public Version Status
New
Public Device Record Key
d9cccec0-478d-4b5a-ae50-2121aebcdcb2

Device Description

Instrument Pouch, 10 in. x 18 in. / 25 cm x 47 cm

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
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 10680651518214
Primary 30680651490446

Customer Contacts