FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Steri-Drape™

DI: 50707387101386 · Model: 1013NS · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

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Basic Information

Brand Name
3M™ Steri-Drape™
Primary DI
50707387101386
Version / Model
1013NS
Catalog Number
1013NS
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2026-04-17
Public Version
1
Public Version Date
2026-04-27
Public Version Status
New
Public Device Record Key
1adee4dd-35b8-43d5-b6c6-94a1131da1ee

Device Description

3M™ Steri-Drape™ X-ray Image Intensifier (C-Arm) Drape 1013NS, 64 inches x 41 inches (165cm x 106cm) Non-sterile

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Unit of Use 00707387101381
Primary 50707387101386

Customer Contacts