← Back to catalogue

Curved Dynablator® XL

FDA UDI

Class II (US FDA UDI)

by RELIGN Corporation

Identity

Trade Name
Curved Dynablator® XL FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI
Device Name
CURVED DYNABLATOR XL FDA UDI
Model / Reference
R-10027 FDA UDI
Description
CURVED DYNABLATOR XL FDA UDI

Identifiers

Catalog Number
R-10027 FDA UDI
Primary DI / UDI-DI
00859273007274 FDA UDI
510(k) Number
K241008 FDA UDI
FDA Product Code
GEI FDA UDI
HRX FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
888.1100 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
MRI Safety
MR Unsafe FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Curved Dynablator® XL by RELIGN Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, 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
RELIGN Corporation

Sources (1)

  • FDA UDI 33e4205a-4e39-4893-b382-addb4de8c106 36 fields · synced Jun 9, 2026