FDA UDI In Commercial Distribution 🇺🇸 United States

Visitec

DI: 30886158106471 · Model: 581724 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Visitec
Primary DI
30886158106471
Version / Model
581724
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-20
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
0bb68b0e-35d6-46d8-8dcb-7a452152b6c0

Device Description

Non-Woven Half Body Aperture Drape with Channel Bag

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Primary 30886158106471
Unit of Use 00886158106470

Customer Contacts

Storage Conditions

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