PILLING
- Primary DI
- 24026704714814
- Brand
- PILLING
- Company
- TELEFLEX INCORPORATED
- Model
- IPN007880
- Catalog number
- 506485
- Device description
- STRONGEUR SUCTION IRRIGATOR
- Published
- 2020-09-04
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| GBX | CATHETER, IRRIGATION |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GBX | Catheter, Irrigation | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 14026704714817 | Direct Marking | GS1 | 0 | |
| 24026704714814 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 14026704714817 | 14026704714817 |
| 24026704714814 | 24026704714814 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical irrigation/aspiration handpiece, reusable | A hand-held device designed to be connected to a separate cannula/tip for both irrigation and aspiration of a surgical site by regulating and directing a stream of pressurized fluid (e.g., sterile water) to the site and facilitating suction of debris from the site. It is activated by the operator, typically through a push-type control(s); it may include connection tubing, however other associated devices (e.g., cannula/tip, clamps, filters, spikes) are not included (i.e., it is neither a tubing set nor an irrigation/aspiration cannula). It is typically intended for an ear/nose/throat (ENT) procedure or neurosurgical use; it is not an ophthalmic device. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 9 | Inch |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(919)544-8000 | CS@TELEFLEX.COM |
Regulatory Flags
- DUNS number
- 002348191
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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