Identity
- Trade Name
- Ranger™ FDA UDI
- Generic Name
- Conduction blood/fluid warmer FDA UDI
- Device Name
- 3M™ Ranger™ Fluid Warming Unit, Model 297, 120V-ENG-E, Refurbished , 1 each, 29700 FDA UDI
- Model / Reference
- 29700 FDA UDI
- Description
- 3M™ Ranger™ Fluid Warming Unit, Model 297, 120V-ENG-E, Refurbished , 1 each, 29700 FDA UDI
Identifiers
- Catalog Number
- 29700 FDA UDI
- Primary DI / UDI-DI
- 00707387781873 FDA UDI
- 510(k) Number
- K060939 FDA UDI
- FDA Product Code
- LHC FDA UDI
- GMDN Term
- Conduction blood/fluid warmer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5950 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Conduction blood/fluid warmer
Ranger™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Conduction blood/fluid warmer.
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Cleared under the same submission
K060939 also covers:
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 970d19f9-b1db-4e8d-b957-1eb0288d682f 36 fields · synced May 30, 2026