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Peak Medical

FDA UDI

Class II (US FDA UDI)

by PEAK MEDICAL Distribution Inc

Identity

Trade Name
PEAK MEDICAL FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
ENDO CABOT NEEDLE HOLDER LAPAROSCOPIC STRAIGHT T/C NEEDLE HOLDER ACCORDING TO SEMM STAINLESS STEEL SHAFT, SCISSOR STYLE RING HANDEL W / SPRING FDA UDI
Model / Reference
335250538 FDA UDI
Description
ENDO CABOT NEEDLE HOLDER LAPAROSCOPIC STRAIGHT T/C NEEDLE HOLDER ACCORDING TO SEMM STAINLESS STEEL SHAFT, SCISSOR STYLE RING HANDEL W / SPRING FDA UDI

Identifiers

Primary DI / UDI-DI
G4533352505380 FDA UDI
FDA Product Code
GCI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Rigid endoscopic tissue manipulation forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, 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 f6f80bd2-910e-4aae-9b82-e706c9f42660 33 fields · synced Jun 8, 2026