FDA UDI In Commercial Distribution 🇺🇸 United States

Cystometry Pack

DI: 00627825007382 · Model: 9021T1051 · Laborie Medical Technologies Canada ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cystometry Pack
Primary DI
00627825007382
Version / Model
9021T1051
Company Name
Laborie Medical Technologies Canada ULC
Labeler DUNS
203383526
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
20f60fe8-4a42-41d8-87c7-5b8724906467

Device Description

with Rectal Split Balloon with Introducer, 6F

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FEN DEVICE, CYSTOMETRIC, HYDRAULIC

GMDN Terms

Code Name
62244 Urodynamic manometric catheter, non-electronic

Identifiers

Type ID
Package 10627825007396
Primary 00627825007382