FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196738953 · Model: MDS9388LF · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196738953
Version / Model
MDS9388LF
Catalog Number
MDS9388LF
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-09
Public Version
1
Public Version Date
2022-04-18
Public Version Status
New
Public Device Record Key
3b28b38e-f735-40be-858e-b8bcf864a4b0

Device Description

ANEROID,HAND HELD,LRG ADULT,NEOPRENE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXQ blood pressure cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Primary 10080196738953

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071244 000
K161035 000
K761302 000