Identity
- Trade Name
- Needless Transfer Device FDA UDI
- Generic Name
- Fluid transfer set, general-purpose FDA UDI
- Device Name
- Needleless Transfer Device w150mic m Filter FDA UDI
- Model / Reference
- 7070109 FDA UDI
- Description
- Needleless Transfer Device w150mic m Filter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290108240955 FDA UDI
- FDA Product Code
- LHI FDA UDI
- GMDN Term
- Fluid transfer set, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Needless Transfer Device by West Pharma. Services Il, . Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- West Pharma. Services Il, . Ltd
Sources (1)
- FDA UDI 6b4fb49b-b3a9-4cdd-9e12-e487c93a6ff9 34 fields · synced May 30, 2026