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Reus, Nk Spo2 Snsr, 39", W Wrap

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
REUS,NK SPO2 SNSR,39",W WRAP FDA UDI
Generic Name
Pulse oximeter probe, reusable FDA UDI
Device Name
REUS,NK SPO2 SNSR,39",W WRAP FDA UDI
Model / Reference
CSW027DN FDA UDI
Description
REUS,NK SPO2 SNSR,39",W WRAP FDA UDI

Identifiers

Catalog Number
28192 FDA UDI
Primary DI / UDI-DI
00840828187688 FDA UDI
510(k) Number
K103685 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pulse oximeter probe, reusable

Reus, Nk Spo2 Snsr, 39", W Wrap by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fbe81844-7acb-40cf-8ee4-002f604ce4c7 36 fields · synced May 30, 2026