← Back to catalogue

Enseal

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref NSLG2S35

by Ethicon Endo-Surgery, LLC

Identity

Trade Name
Enseal EUDAMEDFDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
Enseal Laparoscopic Tissue Sealer G2 Straight Jaw for use with G2 Generator 5mm Diameter 35cm Shaft length FDA UDI
Model / Reference
NSLG2S35 EUDAMEDFDA UDI
Description
Enseal Laparoscopic Tissue Sealer G2 Straight Jaw for use with G2 Generator 5mm Diameter 35cm Shaft length FDA UDI

Identifiers

Catalog Number
NSLG2S35 FDA UDI
Primary DI / UDI-DI
D-USMF000013107000017MC EUDAMED
10705036014188 FDA UDI
Basic UDI-DI
B-USMF000013107000017MC EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
K0201010201,K0201010202 EUDAMED
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Enseal by Ethicon Endo-Surgery, LLC — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000013107
Authorised Representative
Johnson & Johnson Medical GmbH DE-AR-000007712

Sources (2)

  • EUDAMED 3ebef417-7771-4d93-8ab6-97070b153834 61 fields · synced Jul 19, 2026
  • FDA UDI 4e77dd98-445c-459a-8178-5b9aea0cb8a1 36 fields · synced May 30, 2026