Davol Delee Tracheal Suction Catheter
- Primary DI
- 10801741050579
- Brand
- Davol Delee Tracheal Suction Catheter
- Company
- C. R. Bard, Inc.
- Model
- 0118150
- Catalog number
- 0118150
- Device description
- Davol Suction Catheter X-Ray Opaque Rubber
- Published
- 2020-09-21
- 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 |
|---|---|
| BSY | CATHETERS, SUCTION, TRACHEOBRONCHIAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| BSY | Catheters, Suction, Tracheobronchial | Anesthesiology | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10801741050579 | Package | GS1 | 100 | In Commercial Distribution |
| 00801741050572 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10801741050579 | 10801741050579 | ||
| 00801741050572 | 00801741050572 | 801741050572 | 0801741050572 |
GMDN Terms#
| Term | Definition |
|---|---|
| Airway suction catheter | A flexible tube designed to be inserted through the mouth, artificial airway, tracheostomy tube, and/or nostrils, for periodic aspiration of liquids and/or semi-solids from a patient's airway (e.g., pharynx, trachea, bronchi, nasal cavity) as part of a suction system; it is not intended to inflate the lungs. It is typically made of polymer with a smooth and rounded distal-tip, often including end and side holes and a finger-controlled valve to regulate suction. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep away from sunlight |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)526-4455 | medical.services@crbard.com |
Regulatory Flags#
- DUNS number
- 016898496
- 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
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- true
- No natural rubber latex
- false
- Sterilization required before use
- false
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