FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651489396 · Model: 48939 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

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Basic Information

Brand Name
Halyard
Primary DI
30680651489396
Version / Model
48939
Catalog Number
48939
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2024-04-05
Public Version
1
Public Version Date
2024-04-15
Public Version Status
New
Public Device Record Key
76e15bb5-3ce7-4b64-a9f5-85bef5d9c00f

Device Description

Pacemaker Drape

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
Yes
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
Unit of Use 10680651489392
Primary 30680651489396

Customer Contacts