FDA UDI In Commercial Distribution 🇺🇸 United States

Visidrape

DI: 30886158007761 · Model: 581721 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Visidrape
Primary DI
30886158007761
Version / Model
581721
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-04-14
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
ed6e5518-c883-4da9-ad71-ffcccbd2c468

Device Description

Osher Half body Aperture Drape

Device Characteristics

Single Use
Yes
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
Yes
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 30886158007761
Unit of Use 00886158007760

Customer Contacts

Storage Conditions

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