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Greenlight

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
GREENLIGHT FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
INTERNAL SHEATH LASER THERAPY color code green, SL 209mm, oval, slanted distal end, stainless steel, continuous irrigation, compatible with outer sheath 8632026, working insert 8632914, attachment 8632264, and telescopes Ø 4mm, 12°/30°, with irrigation stopcock, quick-lock, reusable FDA UDI
Model / Reference
8632027 FDA UDI
Description
INTERNAL SHEATH LASER THERAPY color code green, SL 209mm, oval, slanted distal end, stainless steel, continuous irrigation, compatible with outer sheath 8632026, working insert 8632914, attachment 8632264, and telescopes Ø 4mm, 12°/30°, with irrigation stopcock, quick-lock, reusable FDA UDI

Identifiers

Catalog Number
8632.027 FDA UDI
Primary DI / UDI-DI
04055207018118 FDA UDI
FDA Product Code
FBO FDA UDI
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope sheath, reusable

Greenlight by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI c0a26390-8082-4711-bc6b-1ff692f80327 35 fields · synced May 30, 2026