BD Vacutainer® UltraTouch™ Push Button Blood Collection Set
- Primary DI
- 00382903673926
- Brand
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set
- Company
- BECTON, DICKINSON AND COMPANY
- Model
- 367392
- Catalog number
- 367392
- Device description
- WINGSET PBBCS UTW PP 23X.75 7 LUER
- Published
- 2016-07-28
- 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
Product Codes#
| Code | Name |
|---|---|
| FPA | Set, administration, intravascular |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | General Hospital | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K212724 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30382903673927 | Package | GS1 | 50 | In Commercial Distribution |
| 50382903673921 | Package | GS1 | 4 | In Commercial Distribution |
| 00382903673926 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 30382903673927 | 30382903673927 | ||
| 50382903673921 | 50382903673921 | ||
| 00382903673926 | 00382903673926 | 382903673926 | 0382903673926 |
GMDN Terms#
| Term | Definition |
|---|---|
| Blood collection set, invasive | A collection of devices intended to be used by a healthcare professional, in combination with evacuated blood collection tubes, for the routine collection of multiple blood specimens from a patient, via one venipuncture, for clinical analyses. It consists of a blood collection needle or venous butterfly/scalp vein needle and additional devices that may include tubing, male/female Luer-lock connectors, clamps, and a blood collection tube holder. Blood access is directly through the vein with the needle. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Room Temperature |
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
- false
- Sterilization required before use
- false
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