FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 20680651780366 · Model: 78036 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
150

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Basic Information

Brand Name
Halyard
Primary DI
20680651780366
Version / Model
78036
Catalog Number
78036
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
150
Record Status
Published
Publish Date
2020-08-14
Public Version
2
Public Version Date
2020-09-21
Public Version Status
Update
Public Device Record Key
b363f11e-d24a-46e7-bcb2-38aeb2cc6e81

Device Description

HALYARD* Sequential Sterilization Wrap-H100-36 X 36-91 x 91-36-5-150-0-3 lbs.

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
No
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
FRG Wrap, sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 30680651780363
Primary 20680651780366
Unit of Use 90680651780365

Customer Contacts