FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00883873836330 · Model: 21300 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00883873836330
Version / Model
21300
Catalog Number
21300-008159
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-04
Public Version
3
Public Version Date
2020-05-18
Public Version Status
Update
Public Device Record Key
cb63b754-4dd7-464a-b4bb-cc85098fe381

Device Description

NIBP - TUBING, 6FT, BAYONET, UDI

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
DSK COMPUTER, BLOOD-PRESSURE

GMDN Terms

Code Name
34978 Blood pressure cuff, reusable

Identifiers

Type ID
Primary 00883873836330

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.0 Feet