FDA UDI In Commercial Distribution 🇺🇸 United States

Steri-Drape™

DI: 30707387006939 · Model: 1012 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Steri-Drape™
Primary DI
30707387006939
Version / Model
1012
Catalog Number
1012
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
3da8f3fa-577b-44e6-9b7f-a31952246e3d

Device Description

3M™ Steri-Drape™ Fluoroscope Drape, 10 per Carton / 4 Cartons per Case, 1012

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
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
No

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 50707387006933
Primary 30707387006939
Unit of Use 00707387006938

Customer Contacts