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Radial Jaw™

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref M00513370

by Boston Scientific Corporation

Identity

Trade Name
Radial Jaw™ EUDAMED
Radial Jaw 4 FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
Radial Jaw 4 SC, LC, Jumbo and Pediatric Biopsy Forceps EUDAMED
Single-Use Biopsy Forceps FDA UDI
Model / Reference
M00513370 EUDAMEDFDA UDI
Description
Single-Use Biopsy Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
08714729745624 EUDAMEDFDA UDI
Basic UDI-DI
01915060000000000000039MT EUDAMED
FDA Product Code
FCL FDA UDI
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
876.1075 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Flexible endoscopic biopsy forceps, single-use

Radial Jaw™ by Boston Scientific Corporation — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000004702
Authorised Representative
Boston Scientific Limited IE-AR-000003840

Sources (2)

  • EUDAMED c6c1aef0-51dd-4eb8-8f0c-3ea6b2c0a648 61 fields · synced Jun 18, 2026
  • FDA UDI 37acb77b-866a-465f-9040-e71f02a28a75 34 fields · synced May 30, 2026