FDA UDI In Commercial Distribution 🇺🇸 United States

SCANLAN® Instruments

DI: 00846159036336 · Model: 8008-81N · SCANLAN INTERNATIONAL INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SCANLAN® Instruments
Primary DI
00846159036336
Version / Model
8008-81N
Catalog Number
8008-81N
Company Name
SCANLAN INTERNATIONAL INC
Labeler DUNS
023055619
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-31
Public Version
1
Public Version Date
2025-02-10
Public Version Status
New
Public Device Record Key
a52db0a0-bb32-4f1b-8776-f633f15e514e

Device Description

Scanlan® Loftus™ Two Level ACDF Distractor

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
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00846159036336

Customer Contacts

Phone
651-298-0997