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Peak Med

FDA UDI

Class II (US FDA UDI)

by PEAK MEDICAL Distribution Inc

Identity

Trade Name
PEAK MED FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
AORTA / AORTIC - COMPRESSOR / OCCLUDER W/ 1/2" OD X 1/4" ID SILICONE TUBING FDA UDI
Model / Reference
3324-0405 FDA UDI
Description
AORTA / AORTIC - COMPRESSOR / OCCLUDER W/ 1/2" OD X 1/4" ID SILICONE TUBING FDA UDI

Identifiers

Primary DI / UDI-DI
G4533324040504 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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: Surgical retractor/retraction system blade, reusable

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

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PEAK MEDICAL Distribution Inc

Sources (1)

  • FDA UDI dbeba997-d1bb-417f-a24b-824f43afd1d2 33 fields · synced Jun 6, 2026