FDA UDI In Commercial Distribution 🇺🇸 United States

Bolsters

DI: 10884521113343 · Model: 88868631-12 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bolsters
Primary DI
10884521113343
Version / Model
88868631-12
Catalog Number
88868631-12
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-19
Public Version
1
Public Version Date
2018-09-19
Public Version Status
New
Public Device Record Key
3257657d-ca78-4816-b373-81ac94a3108e

Device Description

Surgical Rubber Tubing

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KGS RETENTION DEVICE, SUTURE

GMDN Terms

Code Name
33519 Suture retention device

Identifiers

Type ID
Package 20884521113340
Primary 10884521113343

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1.75 Inch
Height 0.1875 Inch
Outer Diameter 0.03125 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
;