FDA UDI In Commercial Distribution 🇺🇸 United States

Patient Controlled Intravenous Analgesia Device (PCI)

DI: 09350902000259 · Model: PCI · GO MEDICAL INDUSTRIES PTY. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Patient Controlled Intravenous Analgesia Device (PCI)
Primary DI
09350902000259
Version / Model
PCI
Catalog Number
PCIIVRE5
Company Name
GO MEDICAL INDUSTRIES PTY. LTD.
Labeler DUNS
757634266
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-18
Public Version
4
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
aa86b48b-ead4-4a71-bdcd-900206ae60b7

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
No
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
MEB Pump, Infusion, Elastomeric

GMDN Terms

Code Name
61732 Ambulatory non-insulin infusion pump, mechanical, single-use

Identifiers

Type ID
Package 09350902000273
Primary 09350902000259
Package 09350902000266

Premarket Submissions

Submission Number Supplement Number
K972158 000