Identity
- Trade Name
- Infusion Pouch 500mL FDA UDI
- Generic Name
- Infusion pump tester FDA UDI
- Model / Reference
- 05080-605-0001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 17290109153985 FDA UDI
- FDA Product Code
- MRZ FDA UDI
- GMDN Term
- Infusion pump tester FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 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
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Infusion pump tester
Infusion Pouch 500mL by Eitan Medical 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
- Eitan Medical Ltd
Sources (1)
- FDA UDI 0066f50a-e2f5-498b-97a5-fb1094fd9515 32 fields · synced Jun 7, 2026