ARROW
- Primary DI
- 30801902216480
- Brand
- ARROW
- Company
- TELEFLEX INCORPORATED
- Model
- IPN928616
- Catalog number
- EC-05000
- Device description
- TheraCath(R) Epidural Catheter
- Published
- 2023-10-26
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 20801902216483 | Package | GS1 | 10 | In Commercial Distribution |
| 30801902216480 | Package | GS1 | 2 | In Commercial Distribution |
| 10801902216486 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|
| 20801902216483 | 20801902216483 |
| 30801902216480 | 30801902216480 |
| 10801902216486 | 10801902216486 |
GMDN Terms
| Term | Definition |
|---|
| Epidural anaesthesia set, non-medicated | A collection of devices intended for the administration of an analgesic or anaesthetic agent (not included) to the epidural space for the management of pain. It includes a needle and/or a catheter with additional procedural devices (e.g., syringe, dressings, guidewire, introducer), and may be intended for single- or continuous-administration. It is not intended for intrathecal anaesthesia This is a single-use device. |
Regulatory Flags
- DUNS number
- 002348191
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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
- true
Other Devices From This Company
teleflex.com