← Back to catalogue

Disp Nlcr Compat Spo2 Snsr, Oxmx, Max-N

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
DISP NLCR COMPAT SPO2 SNSR,OXMX,MAX-N FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
DISP NLCR COMPAT SPO2 SNSR,OXMX,MAX-N FDA UDI
Model / Reference
CSA001DN-M300 FDA UDI
Description
DISP NLCR COMPAT SPO2 SNSR,OXMX,MAX-N FDA UDI

Identifiers

Catalog Number
27082 FDA UDI
Primary DI / UDI-DI
00840828184229 FDA UDI
510(k) Number
K103685 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter probe, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pulse oximeter probe, single-use

Disp Nlcr Compat Spo2 Snsr, Oxmx, Max-N 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, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e7f9e012-9a39-4535-941a-e219bd21ef99 36 fields · synced Jun 6, 2026