FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10885632243912 · Model: 48534 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10885632243912
Version / Model
48534
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-05
Public Version
2
Public Version Date
2020-06-15
Public Version Status
Update
Public Device Record Key
0c6d2a56-b9d0-4982-88c1-bb1379feb7b6

Device Description

Sterilization Pouch -Heat Seal Tyvek® -5.75 in. x 328' -150mm x 100m -Flat Reel -PLASMA

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
No
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
FRG Wrap, sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 20885632243919
Primary 10885632243912

Premarket Submissions

Submission Number Supplement Number
K180139 000

Storage Conditions

Type
Special Storage Condition, Specify
Type
Special Storage Condition, Specify
Special Conditions
Avoid direct sunlight, Protect from water damage