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Peak Medical

FDA UDI

Class I (US FDA UDI)

by PEAK MEDICAL Distribution Inc

Identity

Trade Name
PEAK MEDICAL FDA UDI
Generic Name
Exploratory blunt needle, single-use FDA UDI
Device Name
Cannula tip for Automatic Washer Flushing System for Enhanced Flushing of Clear Flush Kerrison. 10/Box: UDI G453CFK100A0 FDA UDI
Model / Reference
CFK-100-A FDA UDI
Description
Cannula tip for Automatic Washer Flushing System for Enhanced Flushing of Clear Flush Kerrison. 10/Box: UDI G453CFK100A0 FDA UDI

Identifiers

Primary DI / UDI-DI
G453CFK100A0 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Exploratory blunt needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Exploratory blunt needle, single-use

Peak Medical by PEAK MEDICAL Distribution Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exploratory blunt needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9ae8d185-594a-45f8-ae8c-64f02b7cae15 33 fields · synced Jun 1, 2026