FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 20680651763536 · Model: 76353 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
7

Basic Information

Brand Name
Halyard
Primary DI
20680651763536
Version / Model
76353
Catalog Number
76353
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
7
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
511e512a-ea60-4f8e-a5e1-7a3ba3d39595

Device Description

C-Section Drape with Attached Leggings 116 in. x 125 in. / 294 cm x 317 cm - Handi-Bin

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
Yes
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
Package 30680651763533
Primary 20680651763536
Unit of Use 90680651763535

Customer Contacts