PILLING
- Primary DI
- 24026704530377
- Brand
- PILLING
- Company
- TELEFLEX INCORPORATED
- Model
- IPN007747
- Catalog number
- 502566
- Device description
- SANDERS VENTURI 15MM SIDEARM
- Published
- 2016-09-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KTI | BRONCHOSCOPE ACCESSORY |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KTI | Bronchoscope Accessory | Ear, Nose, Throat | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04026704451548 | Direct Marking | GS1 | 0 | |
| 24026704530377 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04026704451548 | 04026704451548 | 4026704451548 |
| 24026704530377 | 24026704530377 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical soft-tissue manipulation forceps, alligator, reusable | A long, thin, hand-held manual surgical instrument designed to facilitate grasping and manipulation of soft-tissues/anatomical structures [typically during ear/nose/throat (ENT) surgery]; it is not intended for insertion through an endoscope, nor into the eye, and is not a dedicated biopsy device. Commonly referred to as alligator- or crocodile-forceps, it has a slender body (to allow for restricted access) and small grasping blades which are hinged close to the distal (working) end. It is a metallic device available in various sizes/lengths; some types may include an integrated suction channel. This is a reusable device intended to be sterilized prior to use. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 2 | Inch |
| Width | 2 | 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
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
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| 14026704936905 | WECK | 544254 | 544254 | 2026-10-20 |
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| 14026704936943 | WECK | 544232 | 544232 | 2026-10-20 |
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| 14026704936981 | WECK | 544252 | 544252 | 2026-10-20 |
| 14026704936998 | WECK | 544254 | 544254 | 2026-10-20 |
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| 14026704937001 | WECK | 544240 | 544240 | 2026-03-30 |
| 10841156108441 | ONCONTROL | IPN919012 | 9402-VC-006 | 2022-01-21 |
| 10841156108458 | ONCONTROL | IPN919013 | 9403-VC-006 | 2022-01-21 |
| 10841156108465 | ONCONTROL | IPN919014 | 9407-VC-006 | 2022-01-21 |
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| 10841156108489 | ONCONTROL | IPN919017 | 9425-VC-006 | 2022-01-20 |
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