FDA UDI Not in Commercial Distribution 🇺🇸 United States

GREENLIGHT

DI: 04055207018170 · Model: 8632225 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GREENLIGHT
Primary DI
04055207018170
Version / Model
8632225
Catalog Number
8632.225
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
9
Public Version Date
2024-11-21
Public Version Status
Update
Public Device Record Key
34c3647b-1e53-4b83-81e0-74616ab8da55
Distribution End Date
2023-04-20

Device Description

LASER WORKING ELEMENT PASSIVE 30° closed, round, distal sheath end slanted, compatible with inner sheath 8655.344, and telescopes Ø 4mm, bayonet-cap, reusable

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FBO CYSTOURETHROSCOPE

GMDN Terms

Code Name
61474 General/multiple surgical laser system beam guide, reusable

Identifiers

Type ID
Primary 04055207018170

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Angle 30 degree