FDA UDI
In Commercial Distribution
🇺🇸 United States
Axiom® Atraum™ With ClotStop®
DI: M665111095AT0
·
Model: 111095AT
·
AXIOM MEDICAL, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Axiom® Atraum™ With ClotStop®
- Primary DI
- M665111095AT0
- Version / Model
- 111095AT
- Company Name
- AXIOM MEDICAL, INCORPORATED
- Labeler DUNS
- 094439676
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-09-23
- Public Version
- 2
- Public Version Date
- 2020-06-19
- Public Version Status
- Update
- Public Device Record Key
- f9ca10d8-5e34-4612-a4fc-6086a3d98410
Device Description
Mediastinal Drain, Silicone, Eyes On Sides, With ClotStop®
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 |
|---|---|---|---|---|
| GBS | Catheter, Ventricular, General & Plastic Surgery | General, Plastic Surgery | 878.4200 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 32544 | Mediastinal drainage catheter, non-antimicrobial | A tube designed to establish a channel for the removal of fluid or purulent material from the mediastinum (the central compartment of the thoracic cavity); it is not coated with an antimicrobial agent. It is typically used in conjunction with, or as a component of, a drainage system that uses a low negative pressure through the drain lumen. It is typically made of silicone, available in various designs, shapes, and sizes, and may include disposable devices dedicated to catheter introduction; it does not include any fluid collection bags/containers. This is a single-use device. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | M665111095AT3 | HIBCC | Case | 10 | In Commercial Distribution | |
| Package | M665111095AT1 | HIBCC | Box | 10 | In Commercial Distribution | |
| Primary | M665111095AT0 | HIBCC |
Customer Contacts
- Phone
- 310-533-9020
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K883887 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 9 mm |