FDA UDI In Commercial Distribution 🇺🇸 United States

AMCO

DI: 00853258006009 · Model: 5L500 · Amco International Manufacturing & Design, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMCO
Primary DI
00853258006009
Version / Model
5L500
Catalog Number
5L500
Company Name
Amco International Manufacturing & Design, Inc.
Labeler DUNS
830424854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-14
Public Version
4
Public Version Date
2022-01-05
Public Version Status
Update
Public Device Record Key
3d72eda5-0f4e-41a5-9afc-4db0e9254fb1

Device Description

Lithium replacement battery for Physio-Control LifePak 500(TM) AED

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MKJ Automated External Defibrillators (Non-Wearable)

GMDN Terms

Code Name
38558 Primary battery

Identifiers

Type ID
Primary 00853258006009

Customer Contacts

Phone
7183888668

Premarket Submissions

Submission Number Supplement Number
K072596 000