FDA UDI Not in Commercial Distribution 🇺🇸 United States

ACUCISE® PROCEDURAL PACK FEMALE PACK B

DI: 20607915128191 · Model: BK024 · 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 B
Primary DI
20607915128191
Version / Model
BK024
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
d5010b60-0681-44dd-b54c-df0bc402fca2
Distribution End Date
2018-10-28

Device Description

Kit Contains: B1005, ACUCISE® ENDOPYELOTOMY SYSTEM B3301, STENT, C-FLEX, 7/10F X 26CM 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
KNY Accessories, Catheter, G-U
DXT Injector And Syringe, Angiographic
EZB Stylet For Catheter, Gastro-Urology
EYB Catheter, Ureteral, Gastro-Urology
FED Endoscopic Access Overtube, Gastroenterology-Urology
FAD Stent, Ureteral
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 20607915128191

Customer Contacts