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AutoTouch Connect reusable autoinjector
FDA UDIClass II (US FDA UDI)
by Amgen Inc.
Identity
- Trade Name
- AutoTouch Connect reusable autoinjector FDA UDI
- Generic Name
- Empty self-injector, mechanical FDA UDI
- Device Name
- AutoTouch Connect reusable autoinjector with optional Bluetooth wireless feature for use with Enbrel Mini (etanercept) single-dose prefilled cartridge FDA UDI
- Model / Reference
- 9006940 FDA UDI
- Description
- AutoTouch Connect reusable autoinjector with optional Bluetooth wireless feature for use with Enbrel Mini (etanercept) single-dose prefilled cartridge FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00358406480019 FDA UDI
- FDA Product Code
- NSC FDA UDI
- GMDN Term
- Empty self-injector, mechanical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Empty self-injector, mechanical
AutoTouch Connect reusable autoinjector by Amgen Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Amgen Inc.
Sources (1)
- FDA UDI fc3559bf-b842-45cd-aa53-3628f625cd60 34 fields · synced May 31, 2026