FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00883873824702 · Model: 11131 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00883873824702
Version / Model
11131
Catalog Number
11131-000001
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-16
Public Version
2
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
3d6373c9-f0a0-4696-8a1b-8fe26559a81d

Device Description

ASSY,PADDLE,INTERNAL HANDLE,REPLACEMENT RESIN,CE

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Hydrogen Peroxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
LDD Dc-defibrillator, low-energy, (including paddles)

GMDN Terms

Code Name
34943 Internal defibrillation electrode, adult, reusable

Identifiers

Type ID
Previous 00681490583275
Primary 00883873824702

Customer Contacts