ARROW
- Primary DI
- 20801902198123
- Brand
- ARROW
- Company
- TELEFLEX INCORPORATED
- Model
- IPN920819
- Catalog number
- SI-09600
- Device description
- Arterial Catheterization Set
- Published
- 2023-06-12
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DYB | Introducer, catheter |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DYB | Introducer, Catheter | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K780532 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20801902198123 | Package | GS1 | 10 | In Commercial Distribution |
| 10801902198126 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20801902198123 | 20801902198123 |
| 10801902198126 | 10801902198126 |
GMDN Terms#
| Term | Definition |
|---|---|
| Peripheral artery cannula | A short, thin tube intended for short-term (<= 30 days) percutaneous access to a peripheral artery for invasive blood pressure monitoring and arterial blood sampling; it may in addition be intended for peripheral IV and/or subcutaneous administration of fluid/medication. Also referred to as a peripheral arterial catheter, it is used with an external blood pressure transducer (not included) to enable pressures to be measured; it does not include electronic sensors and is not intended for thermal dilution techniques. It may include devices dedicated to introduction/function (e.g., introducer needle, guidewire, adaptor). This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(919)544-8000 | CS@TELEFLEX.COM |
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
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10841495149457 | QUIKCLOT | 183 | 183 | 2026-07-17 |
| 10841495149464 | QUIKCLOT | 183 | 183 | 2026-07-17 |
| 10841495149471 | QUIKCLOT | 188 | 188 | 2026-07-17 |
| 10841495149488 | QUIKCLOT | 188 | 188 | 2026-07-17 |
| 10841495149495 | QUIKCLOT | 374 | 374 | 2026-07-17 |
| 10841495149501 | QUIKCLOT | 374 | 374 | 2026-07-17 |
| 10841495149518 | QUIKCLOT | 458 | 458 | 2026-07-17 |
| 10841495149549 | QUIKCLOT | 459 | 459 | 2026-07-17 |
| 10841495149563 | QUIKCLOT | 460 | 460 | 2026-07-17 |
| 10841495149587 | QUIKCLOT | 461 | 461 | 2026-07-17 |
| 10841495149600 | QUIKCLOT | 467Z | 467Z | 2026-07-17 |
| 10841495149624 | QUIKCLOT | 487 | 487 | 2026-07-17 |
| 14026704930644 | QUIKCLOT | 183 | 183 | 2026-07-17 |
| 14026704930651 | QUIKCLOT | 183 | 183 | 2026-07-17 |
| 14026704930668 | QUIKCLOT | 188 | 188 | 2026-07-17 |
| 14026704930675 | QUIKCLOT | 188 | 188 | 2026-07-17 |
| 14026704930682 | QUIKCLOT | 374 | 374 | 2026-07-17 |
| 14026704930699 | QUIKCLOT | 374 | 374 | 2026-07-17 |
| 14026704930705 | QUIKCLOT | 458 | 458 | 2026-07-17 |
| 14026704930729 | QUIKCLOT | 459 | 459 | 2026-07-17 |
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| 10884450119799 | Prelude EASE™ | Merit Medical Systems, Inc. | DYB | 2026-06-09 |
| 10884450114855 | Prelude IDeal™ | Merit Medical Systems, Inc. | DYB | 2026-06-08 |
| 00850084947001 | Genie MAX | CULTIV8 1, LLC | DYB | 2026-05-29 |
| G440VIZ1750 | Multiflex | Vizaramed, Inc. | DYB | 2026-04-09 |
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