Identity
- Trade Name
- 3M™ Ranger™ FDA UDI
- Generic Name
- Intravenous pressure infusor, manual, reusable FDA UDI
- Device Name
- 3M™ Ranger™ Pressure Infusor 14500, 120V-ENG-B , Model 145 FDA UDI
- Model / Reference
- 14500 FDA UDI
- Description
- 3M™ Ranger™ Pressure Infusor 14500, 120V-ENG-B , Model 145 FDA UDI
Identifiers
- Catalog Number
- 14500 FDA UDI
- Primary DI / UDI-DI
- 00707387781163 FDA UDI
- FDA Product Code
- KZD FDA UDI
- GMDN Term
- Intravenous pressure infusor, manual, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5420 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intravenous pressure infusor, manual, reusable
3M™ Ranger™ by 3m Company — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI 112cf02a-7187-498b-a983-595fa6c6257a 35 fields · synced May 30, 2026