FDA UDI Not in Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651019012 · Model: 01901 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
Halyard
Primary DI
30680651019012
Version / Model
01901
Catalog Number
ACM1901
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2019-10-23
Public Version
2
Public Version Date
2024-07-09
Public Version Status
Update
Public Device Record Key
9def8391-194e-43e7-a037-b83c4427b285
Distribution End Date
2024-03-29

Device Description

BAPTIST LIVER LEFT SIDE

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 30680651019012
Unit of Use 90680651019014

Customer Contacts