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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
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
MIS DeBakey Forceps - Straight 1mm jaws, 5mm Shaft, 6.75" (17cm) Working Length, Round Squeeze Handle, Stainless Steel, 11.75" (30cm) FDA UDI
Model / Reference
511-8598.1 FDA UDI
Description
MIS DeBakey Forceps - Straight 1mm jaws, 5mm Shaft, 6.75" (17cm) Working Length, Round Squeeze Handle, Stainless Steel, 11.75" (30cm) FDA UDI

Identifiers

Primary DI / UDI-DI
G453511859810 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable 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: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20dc9acf-8b22-480a-b38a-f7caf6cc7452 33 fields · synced Jun 1, 2026