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Heartline Debakey Grasper

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEARTLINE DEBAKEY GRASPER FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
HEARTLINE DEBAKEY GRASPER CURVED TO SIDE 1x2 JAW FDA UDI
Model / Reference
2800-7822 FDA UDI
Description
HEARTLINE DEBAKEY GRASPER CURVED TO SIDE 1x2 JAW FDA UDI

Identifiers

Catalog Number
2800-7822 FDA UDI
Primary DI / UDI-DI
00192896007253 FDA UDI
510(k) Number
K152400 FDA UDI
FDA Product Code
GCJ 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 24 Centimeter FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

Heartline Debakey Grasper by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8d90d091-0790-479b-8802-898d8f2a7144 37 fields · synced Jun 1, 2026