FDA UDI
In Commercial Distribution
🇺🇸 United States
MP Vial Adapter 13mm
DI: 37290108240796
·
Model: 8070149
·
WEST PHARMA. SERVICES IL, . LTD
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- MP Vial Adapter 13mm
- Primary DI
- 37290108240796
- Version / Model
- 8070149
- Company Name
- WEST PHARMA. SERVICES IL, . LTD
- Labeler DUNS
- 600267793
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2017-06-06
- Public Version
- 9
- Public Version Date
- 2020-07-23
- Public Version Status
- Update
- Public Device Record Key
- 130012eb-b736-4ed9-9d89-0fc70fdfe9c0
Device Description
MP Vial Adapter 13mm FLL – VF 3 Pack
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Radiation Sterilization
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LHI | Set, I.V. Fluid Transfer | General Hospital | 880.5440 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 60539 | Vial/bottle adaptor, non-hermetic | A device intended to be fitted to a vial or bottle to enable the removal of its contents, (e.g., medication, nutritional solution for enteral feeding) into a syringe, for subsequent administration to a patient. It is typically a housing with a barbed connection or spike that attaches to or replaces the container lid, and a small bore connection (typically ENFit or a Luer); it does not allow for pressure equalization/airtight transfer of contents. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 27290108240799 | GS1 | 3 | In Commercial Distribution | ||
| Package | 17290108240792 | GS1 | 80 | In Commercial Distribution | ||
| Primary | 37290108240796 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K130179 | 000 |