FDA UDI
In Commercial Distribution
🇺🇸 United States
Ultipor™ Anesthesia Breathing Circuit System - Patient Kit
DI: 00636207315311
·
Model: VMPKLA
·
Global Life Sciences Solutions USA LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- Ultipor™ Anesthesia Breathing Circuit System - Patient Kit
- Primary DI
- 00636207315311
- Version / Model
- VMPKLA
- Catalog Number
- VMPKLA
- Company Name
- Global Life Sciences Solutions USA LLC
- Labeler DUNS
- 011658242
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-06-29
- Public Version
- 4
- Public Version Date
- 2024-02-29
- Public Version Status
- Update
- Public Device Record Key
- e63e805b-6d6a-4d9e-93d2-d3077d76a961
Device Description
Large Vanilla-Scented Adult Face Mask, Ported Elbow, and Ultipor 25 Filter
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
- Yes
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| CAH | Filter, bacterial, breathing-circuit | Anesthesiology | 868.5260 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 62128 | Patient-end respiratory anaesthesia kit | A collection of non-sterile devices intended to create a hygienic connection between a patient’s airway and an anaesthesia breathing circuit. It is primarily intended for use with a reusable breathing circuit and typically includes an anaesthesia mask, a tube/mask breathing circuit connector and a microbial medical gas filter. This is a single-patient reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 30636207315312 | GS1 | case | 20 | In Commercial Distribution | |
| Primary | 00636207315311 | GS1 |
Customer Contacts
- Phone
- +1(800)645-6578 ext. 5164843600
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K013093 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | Minimizes viral and bacterial contamination of the inspiratory and expiratory limbs of the circuit with a minimum efficiency of 99.999%. |