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Minilap

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
MINILAP FDA UDI
Generic Name
Rigid endoscopic grasping forceps, single-use FDA UDI
Device Name
Tong Grasper FDA UDI
Model / Reference
IPN002706 FDA UDI
Description
Tong Grasper FDA UDI

Identifiers

Catalog Number
PGBC300 FDA UDI
Primary DI / UDI-DI
14026704582638 FDA UDI
510(k) Number
K113597 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic grasping forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 300 Millimeter FDA UDI

Category: Rigid endoscopic grasping forceps, single-use

Minilap by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic grasping forceps, single-use.

Cleared under the same submission

K113597 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 9cffa3f4-397f-44a0-a6ad-ed1c2abb891f 37 fields · synced May 30, 2026