FDA UDI
In Commercial Distribution
🇺🇸 United States
IV Catheter
DI: 00853620005180
·
Model: 035662588000
·
Merit Pharmaceutical
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
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Basic Information
- Brand Name
- IV Catheter
- Primary DI
- 00853620005180
- Version / Model
- 035662588000
- Company Name
- Merit Pharmaceutical
- Labeler DUNS
- 093370369
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-01-01
- Public Version
- 2
- Public Version Date
- 2024-03-11
- Public Version Status
- Update
- Public Device Record Key
- 38d83f19-6789-45e6-ba14-7af78ed3f42c
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
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | General Hospital | 880.5200 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 40601 | Peripheral vascular catheter | A sterile, thin, flexible tube intended to be inserted into the peripheral vasculature of a patient to enable short-term (< 30 days) intravascular access; it is not intended to be advanced to the central vasculature. It typically includes dedicated accessories to facilitate catheter introduction/placement and function (e.g., connectors, injection ports, stylet and/or wings for fixation). It may be used for blood sampling, monitoring of blood pressure, to administer fluids, medication and/or for the injection of contrast media. This is a single-use device. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 10853620005187 | GS1 | 50 | In Commercial Distribution | ||
| Primary | 00853620005180 | GS1 | ||||
| Package | 20853620005184 | GS1 | 4 | In Commercial Distribution |
Customer Contacts
- Phone
- (323) 227-4831
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K071382 | 000 |