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Ranger™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Ranger™ FDA UDI
Generic Name
Conduction blood/fluid warmer set FDA UDI
Device Name
3M™ Ranger™ Hose Cap, 12 per Case, 90026 FDA UDI
Model / Reference
90026 FDA UDI
Description
3M™ Ranger™ Hose Cap, 12 per Case, 90026 FDA UDI

Identifiers

Catalog Number
90026 FDA UDI
Primary DI / UDI-DI
50707387781922 FDA UDI
FDA Product Code
KZL FDA UDI
GMDN Term
Conduction blood/fluid warmer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9205 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Conduction blood/fluid warmer set

Ranger™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conduction blood/fluid warmer set.

Cleared under the same submission

BK940032 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 6577a87f-0328-4444-aaed-3b27d74af819 36 fields · synced Jun 6, 2026