FDA UDI Not in Commercial Distribution 🇺🇸 United States

ACUCISE® PROCEDURAL PACK FEMALE PACK A

DI: 20607915128184 · Model: BK023 · APPLIED MEDICAL RESOURCES CORPORATION
Product Codes
8
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACUCISE® PROCEDURAL PACK FEMALE PACK A
Primary DI
20607915128184
Version / Model
BK023
Company Name
APPLIED MEDICAL RESOURCES CORPORATION
Labeler DUNS
187129135
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-09
Public Version
4
Public Version Date
2019-02-08
Public Version Status
Update
Public Device Record Key
d28fb95d-b7ce-4c95-9c27-78850a2ff1c7
Distribution End Date
2018-10-28

Device Description

Kit Contains: B1005, ACUCISE® ENDOPYELOTOMY SYSTEM B3304, STENT, C-FLEX 7/10F x 24 CM B7076, FORTE AxP SET 12/14/18F 28CM 6/BX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FED Endoscopic Access Overtube, Gastroenterology-Urology
FAD Stent, Ureteral
KNY Accessories, Catheter, G-U
EZB Stylet For Catheter, Gastro-Urology
DXT Injector And Syringe, Angiographic
EYB Catheter, Ureteral, Gastro-Urology
FZP Clip, Implantable
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
47053 Ureteral stent-placement set
58005 Polymeric ureteral stent
34926 Ureteral catheter
46691 Gastro-urological guidewire, single-use

Identifiers

Type ID
Primary 20607915128184

Customer Contacts