FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD9152191030 · Model: SD915219103 · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD9152191030
Version / Model
SD915219103
Catalog Number
SD915219103
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-16
Public Version
1
Public Version Date
2023-02-24
Public Version Status
New
Public Device Record Key
19811d97-3225-4ebc-951e-5a9073626328

Device Description

2 3/4 Inch Distractor Drill Guide, Left, 8mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
48025 Orthopaedic bone-fragment manipulator, reusable

Identifiers

Type ID
Primary B382SD9152191030

Customer Contacts