FDA UDI Not in Commercial Distribution 🇺🇸 United States

Hopkins

DI: 00634782034702 · Model: 760HOPLF · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Hopkins
Primary DI
00634782034702
Version / Model
760HOPLF
Catalog Number
760HOPLF
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-21
Public Version
3
Public Version Date
2019-04-12
Public Version Status
Update
Public Device Record Key
5a9183a0-41e7-4f95-9c47-3550a3f8ca3a
Distribution End Date
2019-04-11

Device Description

Pocket Aneroid Sphyg,Adult, Black, HOP PL, LF

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
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
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Package 00634782534554
Primary 00634782034702

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult, 23-40cm

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-4 – 131 Degrees Fahrenheit