FDA UDI In Commercial Distribution 🇺🇸 United States

MYELO-NATE

DI: H67140110150 · Model: Procedure Kit · UTAH MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MYELO-NATE
Primary DI
H67140110150
Version / Model
Procedure Kit
Catalog Number
4011015
Company Name
UTAH MEDICAL PRODUCTS, INC.
Labeler DUNS
094651270
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-04
Public Version
1
Public Version Date
2020-06-12
Public Version Status
New
Public Device Record Key
8bbc7502-1498-4e03-89ef-fa54d11b7486

Device Description

MYELONATE KIT (1") 22GA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
12404 Lumbar puncture kit

Identifiers

Type ID
Primary H67140110150
Package H67140110151

Customer Contacts

Phone
800-533-4984