FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651789656 · Model: 78965 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
120

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Basic Information

Brand Name
Halyard
Primary DI
30680651789656
Version / Model
78965
Catalog Number
78965
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2019-10-07
Public Version
1
Public Version Date
2019-10-15
Public Version Status
New
Public Device Record Key
ed0cc474-2fbd-4909-8acc-58921f82015b

Device Description

Utility Drape 35 in. x 62 in. / 90 cm x 157 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
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
47782 Patient surgical drape, single-use, non-sterile

Identifiers

Type ID
Primary 30680651789656
Unit of Use 90680651789658

Customer Contacts