Hyperbaric Kit
- Primary DI
- 20886333203080
- Brand
- Hyperbaric Kit
- Company
- ARGON MEDICAL DEVICES, INC.
- Model
- 049964906B
- Catalog number
- 049964906B
- Device description
- Hyperbaric Kit
- Published
- 2016-09-20
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| OJA | Intravenous Extension Tubing Set |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| OJA | Intravenous Extension Tubing Set | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20886333203080 | Package | GS1 | 20 | In Commercial Distribution |
| 00886333203086 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20886333203080 | 20886333203080 | ||
| 00886333203086 | 00886333203086 | 886333203086 | 0886333203086 |
GMDN Terms
| Term | Definition |
|---|---|
| Angiography kit | A collection of sterile devices and equipment used to prepare a patient for the radiographic visualization of the arteries of a particular organ system or body part through the vascular injection of contrast media. It typically includes a combination of fluid/contrast media administration devices (e.g., tubing, manifold, stopcocks, and syringes) and/or dedicated angiography supportive devices (e.g., angiography drapes, covers, dressings); the angiography catheter is not included. This is a single-use device. |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| 1.800.927.4669 | Customer.Service@argonmedical.com |
Regulatory Flags
- DUNS number
- 140727624
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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