FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 04055207020555 · Model: 8781033 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04055207020555
Version / Model
8781033
Catalog Number
8781033
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
7
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
9a8d9f82-ef44-442e-a53d-b263562e5134
Distribution End Date
2019-11-05

Device Description

TUBE F.TELESCOPE 8781403 Ø 15MM WL 195MM 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
["Hydrogen Peroxide", "Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 04055207020555

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Outer Diameter 15 Millimeter
Length 195 Millimeter