FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04055207039175 · Model: 826721 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04055207039175
Version / Model
826721
Catalog Number
8267.21
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-21
Public Version
2
Public Version Date
2024-11-21
Public Version Status
Update
Public Device Record Key
bbbdf64c-abcc-4bf4-8f36-15b129d44f89

Device Description

PROBE DULL TL 265MM angled

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
Yes
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
KAK PROBE, ENT

GMDN Terms

Code Name
44067 ENT surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 04055207039175

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Length 265 Millimeter