FDA UDI
In Commercial Distribution
🇺🇸 United States
Axiom®
DI: M6651018250
·
Model: 101825
·
AXIOM MEDICAL, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Axiom®
- Primary DI
- M6651018250
- Version / Model
- 101825
- Company Name
- AXIOM MEDICAL, INCORPORATED
- Labeler DUNS
- 094439676
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-23
- Public Version
- 4
- Public Version Date
- 2018-07-06
- Public Version Status
- Update
- Public Device Record Key
- e0bdd410-9c0e-4682-9294-6fa2ca48a023
Device Description
Penrose Tubing, Silicone
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 |
|---|---|---|---|---|
| KDH | Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration | Gastroenterology, Urology | 876.5980 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 43437 | Surgical capillary wound drain, luminal, synthetic polymer | A sterile device with a lumen(s) designed to establish a passive egress for the removal of fluid (drainage of blood, lymph, exudate) from a surgical wound to minimize its accumulation and risk of wound infection; it is not dedicated to a particular anatomical wound. It is typically inserted into the wound by a surgeon in the operating room (OR) after the completion of an inpatient or outpatient procedure. It is typically made of radiopaque silicone and is available in various forms (e.g., Penrose type, tubular with side holes, multi-tubular). This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | M6651018253 | HIBCC | Case | 10 | In Commercial Distribution | |
| Package | M6651018251 | HIBCC | Box | 10 | In Commercial Distribution | |
| Primary | M6651018250 | HIBCC |
Customer Contacts
- Phone
- 310-533-9020
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K781749 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 18 | Inch | |
| Lumen/Inner Diameter | 0.25 | Inch |