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Good Neighbor

FDA UDI

Class II (US FDA UDI)

by Amerisourcebergen Drug Corporation

Identity

Trade Name
Good Neighbor FDA UDI
Generic Name
Pulse oximeter probe, reusable FDA UDI
Device Name
Good Neighbor Pharmacy Deluxe Pulse Oximeter FDA UDI
Model / Reference
90-50D FDA UDI
Description
Good Neighbor Pharmacy Deluxe Pulse Oximeter FDA UDI

Identifiers

Primary DI / UDI-DI
00087701427404 FDA UDI
510(k) Number
K082641 FDA UDI
FDA Product Code
OCH 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

No

FDA UDI

Over-the-Counter

Yes

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: Pulse oximeter probe, reusable

Good Neighbor by Amerisourcebergen Drug Corporation — 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 8ce0aaf4-ce8d-4ad2-ac1c-38545da7ffff 34 fields · synced May 30, 2026