Air-Water Syringe Tip
- Primary DI
- 00616784223230
- Brand
- Air-Water Syringe Tip
- Company
- DYNAREX CORPORATION
- Model
- 2232
- Device description
- Air-Water Syringe Tip Clear
- Published
- 2021-09-01
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| EHZ | Evacuator, Oral Cavity |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| EHZ | Evacuator, Oral Cavity | Dental | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00616784223230 | Package | GS1 | 40 | In Commercial Distribution |
| 00616784223223 | Primary | GS1 | 0 | |
| 00616784223216 | Unit of Use | GS1 | 0 | |
| 00810180843553 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00616784223230 | 00616784223230 | 616784223230 | 0616784223230 |
| 00616784223223 | 00616784223223 | 616784223223 | 0616784223223 |
| 00616784223216 | 00616784223216 | 616784223216 | 0616784223216 |
| 00810180843553 | 00810180843553 | 810180843553 | 0810180843553 |
GMDN Terms
| Term | Definition |
|---|---|
| Dental delivery system irrigation handpiece | A hand-held device that is used to regulate and direct a stream of pressurized, warmed water and/or air for the purpose of irrigating/clearing debris from the field of operation in the oral cavity during restorative or operative dental procedures. It is fitted with a long syringe-like nozzle that is activated by the user, typically through push-type controls. This device, also commonly known as a three-way or a Triplex syringe, is typically a component of a dental delivery system from which the air and water is supplied. This is a reusable device. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 008124539
- Device count
- 250
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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