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9.8mhz Infant Flat Probe

FDA UDI

Class II (US FDA UDI)

by Parks Medical Electronics, Inc.

Identity

Trade Name
9.8MHZ INFANT FLAT PROBE FDA UDI
Generic Name
Noninvasive vascular ultrasound system probe FDA UDI
Model / Reference
832-4980-11 FDA UDI

Identifiers

Primary DI / UDI-DI
00816787023183 FDA UDI
FDA Product Code
JOP FDA UDI
GMDN Term
Noninvasive vascular ultrasound system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2880 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Noninvasive vascular ultrasound system probe

9.8mhz Infant Flat Probe by Parks Medical Electronics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a458420-7974-42fb-9268-4c2b7900d9d3 33 fields · synced May 30, 2026