BD Plastipak
- Primary DI
- 30382903033110
- Brand
- BD Plastipak
- Company
- BECTON, DICKINSON AND COMPANY
- Model
- 303311
- Catalog number
- 303311
- Device description
- SYRINGE 3ML LL PLASTIPAK VACCINATION
- Published
- 2023-11-15
- 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
Related Records
Product Codes
| Code | Name |
|---|---|
| FMF | Syringe, piston |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FMF | Syringe, Piston | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30382903033110 | Package | GS1 | 200 | In Commercial Distribution |
| 50382903033114 | Package | GS1 | 4 | In Commercial Distribution |
| 00382903033119 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 30382903033110 | 30382903033110 | ||
| 50382903033114 | 50382903033114 | ||
| 00382903033119 | 00382903033119 | 382903033119 | 0382903033119 |
GMDN Terms
| Term | Definition |
|---|---|
| General-purpose syringe, single-use | A sterile device consisting of a calibrated barrel (cylinder) with plunger intended to be used for injection/withdrawal of fluids/gas (e.g., medication) to/from a medical device or the body (i.e., capable of both); a needle is not included. It is intended for various medical applications and is not dedicated to medication administration. At the distal end of the barrel is a male connector (typically Luer-lock/slip type) for the attachment to a hypodermic needle or an administration set. It is typically made of plastic and silicone materials and may have anti-stick plunger allowing smooth plunger movement, either manually or by a syringe pump. 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 |
|---|
Regulatory Flags
- DUNS number
- 001292192
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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