FDA UDI In Commercial Distribution 🇺🇸 United States

ReShape Calibration Tubes

DI: 00850007764258 · Model: B-2032 · Reshape Lifesciences Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ReShape Calibration Tubes
Primary DI
00850007764258
Version / Model
B-2032
Catalog Number
B-2032
Company Name
Reshape Lifesciences Inc.
Labeler DUNS
022894714
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-16
Public Version
4
Public Version Date
2023-12-15
Public Version Status
Update
Public Device Record Key
5231a194-e95d-419b-83a4-d1de444dec67

Device Description

Calibration and Sizing Tube 32 French

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
44686 Gastric calibration tube

Identifiers

Type ID
Primary 00850007764258
Previous 00850007764210

Customer Contacts

Phone
844-937-7374

Premarket Submissions

Submission Number Supplement Number
K230131 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged and consult instructions for use