Alaris, SmartSite
- Primary DI
- 10885403233036
- Brand
- Alaris, SmartSite
- Company
- BD Switzerland Sàrl
- Model
- 32400E-07
- Catalog number
- 32400E-07
- Device description
- 44" EXTENSION SET W/STOPCOCK & 2SS
- Published
- 2016-10-17
- Public version status
- Update
- 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 |
|---|---|
| FPA | Set, administration, intravascular |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 50885403233034 | Package | GS1 | 50 | In Commercial Distribution |
| 10885403233036 | Primary | GS1 | 0 |
GMDN Terms
| Term | Definition |
|---|---|
| Intravenous administration tubing extension set | A collection of tubing and connectors intended to establish an extension of tubing where the standard length of the tubing in an intravenous (IV) administration set is insufficient. This is a single-use device. |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Room Temperature |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(844)823-5433 | customer_support@bd.com |
Regulatory Flags
- DUNS number
- 482631558
- 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
- false
- Sterilization required before use
- false
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