FDA UDI In Commercial Distribution 🇺🇸 United States

AcQGuide MAX

DI: 00850027837017 · Model: 900200 · ACUTUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcQGuide MAX
Primary DI
00850027837017
Version / Model
900200
Catalog Number
900200
Company Name
ACUTUS MEDICAL, INC.
Labeler DUNS
844418199
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-08
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
1c99937e-d8b4-4141-9134-c321d067af5f

Device Description

12F AcQGuide MAX 2.0 Steerable Sheath

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DRA Catheter, Steerable

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00850027837017

Customer Contacts