Identity
- Trade Name
- ID Adapter FDA UDI
- Generic Name
- Needle guide, single-use FDA UDI
- Device Name
- Intradermal Adapter FDA UDI
- Model / Reference
- 5070204 FDA UDI
- Description
- Intradermal Adapter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290108240900 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Needle guide, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
Ethylene Oxide FDA UDI
ID Adapter 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 ec4be519-0042-4722-b364-b88b24aa49a5 34 fields · synced May 30, 2026