← Back to catalogue

GreenLight XPS™ Laser System Power Cord

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
GreenLight XPS™ Laser System Power Cord FDA UDI
Generic Name
General/multiple surgical frequency-doubled solid-state laser system FDA UDI
Device Name
Power Cord FDA UDI
Model / Reference
0136-1492 FDA UDI
Description
Power Cord FDA UDI

Identifiers

Primary DI / UDI-DI
08714729987000 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical frequency-doubled solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General/multiple surgical frequency-doubled solid-state laser system

GreenLight XPS™ Laser System Power Cord by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical frequency-doubled solid-state laser system.

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
Boston Scientific

Sources (1)

  • FDA UDI 2ec3de69-3568-4bf1-a02e-bec2a4082b3a 33 fields · synced Jun 6, 2026