FDA UDI In Commercial Distribution 🇺🇸 United States

Wet-Field®

DI: 30886158030318 · Model: 221204 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Wet-Field®
Primary DI
30886158030318
Version / Model
221204
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
8
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
b5e22649-d3fb-4134-affa-352328c415d2

Device Description

Standard Forceps

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Direct Marking 00886158030317
Primary 30886158030318

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place.