FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00724995184209 · Model: 00712809 · US Endoscopy
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00724995184209
Version / Model
00712809
Catalog Number
00712809
Company Name
US Endoscopy
Labeler DUNS
627879687
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-31
Public Version
1
Public Version Date
2021-04-08
Public Version Status
New
Public Device Record Key
4c31448b-d1c5-4ba7-b863-5c949cb7e303

Device Description

The Bite Block Intermediate, Latex Free Strap is used to protect the endoscope insertion tube from being bitten by the patient.

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MNK Endoscopic bite block

GMDN Terms

Code Name
34143 Endoscopic bite block, basic, single-use

Identifiers

Type ID
Package 10724995184206
Primary 00724995184209

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at controlled room temperature