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

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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
8
Public Version Date
2024-11-21
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