← Back to catalogue

Peak Medical

FDA UDI

Class I (US FDA UDI)

by PEAK MEDICAL Distribution Inc

Identity

Trade Name
PEAK MEDICAL FDA UDI
Generic Name
Point aesthesiometer FDA UDI
Device Name
26cm Overall Length, Stainless Steel Pointer for Pain Management w/ Loop Finger Ring (Specs on File). FDA UDI
Model / Reference
3323-1216 FDA UDI
Description
26cm Overall Length, Stainless Steel Pointer for Pain Management w/ Loop Finger Ring (Specs on File). FDA UDI

Identifiers

Primary DI / UDI-DI
G453332312160 FDA UDI
FDA Product Code
FGM FDA UDI
GMDN Term
Point aesthesiometer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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: Point aesthesiometer

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

Similar devices

Also classified as Point aesthesiometer.

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

Manufacturer
PEAK MEDICAL Distribution Inc

Sources (1)

  • FDA UDI 05751dc0-0b01-47f8-b746-f19f8b88543e 33 fields · synced May 30, 2026