← Back to catalogue

EndoGrip

FDA UDI

Class I (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
EndoGrip FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
EndoGrip Grasping Forceps FDA UDI
Model / Reference
1177-01 FDA UDI
Description
EndoGrip Grasping Forceps FDA UDI

Identifiers

Catalog Number
1177-01 FDA UDI
Primary DI / UDI-DI
00816734021521 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use 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

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

Yes

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
Outer Diameter — 2.3 Millimeter FDA UDI
Length — 230 Centimeter FDA UDI
Width — 8.3 Millimeter FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-use

EndoGrip by Diversatek Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Diversatek Healthcare

Sources (1)

  • FDA UDI 0f2b42f1-70ca-4653-9d24-ffc50e209a94 37 fields · synced May 30, 2026