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Enseal

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref NSLX137C

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 X1 Tissue Sealer EUDAMED
ENSEAL X1 Tissue Sealer, Curved Jaw, 37 cm Shaft Length FDA UDI
Model / Reference
NSLX137C EUDAMEDFDA UDI
Description
ENSEAL X1 Tissue Sealer, Curved Jaw, 37 cm Shaft Length FDA UDI

Identifiers

Catalog Number
NSLX137C FDA UDI
Primary DI / UDI-DI
10705036015468 EUDAMEDFDA UDI
Basic UDI-DI
0705036a0008578 EUDAMED
FDA Product Code
HGI FDA UDI
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
884.4120 FDA UDI
878.4400 FDA UDI
Market of Registration
Belgium 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

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 — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 87ba2dec-1d6b-492c-8fa2-9943e18f0150 61 fields · synced Aug 4, 2026
  • FDA UDI 98f4e309-0429-4073-938f-0f1d1b27e21d 36 fields · synced May 30, 2026