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Key Surgical Biopsy Forceps

FDA UDI

Class I (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
Key Surgical Biopsy Forceps FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
Swinging Biopsy Forceps, Alligator Cup with Spike, 2.4mm Diam, 1800mm L FDA UDI
Model / Reference
EN10269AS FDA UDI
Description
Swinging Biopsy Forceps, Alligator Cup with Spike, 2.4mm Diam, 1800mm L FDA UDI

Identifiers

Catalog Number
EN10269AS FDA UDI
Primary DI / UDI-DI
00849771038832 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Key Surgical Biopsy Forceps by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Key Surgical, LLC

Sources (1)

  • FDA UDI 8a10fb4a-1e43-48a5-a515-25efdfa01302 36 fields · synced May 29, 2026