FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 20680651375005 · Model: 37500 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

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Basic Information

Brand Name
Halyard
Primary DI
20680651375005
Version / Model
37500
Catalog Number
37500
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2020-11-16
Public Version
1
Public Version Date
2020-11-24
Public Version Status
New
Public Device Record Key
c27eb1cc-df5f-45a8-9a3f-818d8391b853

Device Description

HALYARD* Soft Circumcision Strap

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
NZD Stretcher, patient restraint

GMDN Terms

Code Name
44851 Limb/torso/head restraint, single-use

Identifiers

Type ID
Package 30680651375002
Primary 20680651375005
Unit of Use 90680651375004

Customer Contacts