FDA UDI In Commercial Distribution 🇺🇸 United States

SBH

DI: 00850068304011 · Model: K123234 · SBH Surgical
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SBH
Primary DI
00850068304011
Version / Model
K123234
Catalog Number
SB 100.040E
Company Name
SBH Surgical
Labeler DUNS
096823436
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-11
Public Version
1
Public Version Date
2024-09-19
Public Version Status
New
Public Device Record Key
875c86e0-90e3-4f77-8689-0dac150c32c4

Device Description

1/1, Sterilization Container Perforated Lid, Blue, 585mm x 278mm, 23" x 11"

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00850068304011

Customer Contacts

Phone
9493053300