FDA UDI In Commercial Distribution 🇺🇸 United States

BREG

DI: 00672736141502 · Model: ASCEND CERV 172, REGULAR, W/O REPL PADS · BREG, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BREG
Primary DI
00672736141502
Version / Model
ASCEND CERV 172, REGULAR, W/O REPL PADS
Catalog Number
SP50172-030
Company Name
BREG, INC.
Labeler DUNS
604483321
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-11
Public Version
1
Public Version Date
2023-09-19
Public Version Status
New
Public Device Record Key
bcfadc0a-701a-4b55-a07c-85eea59c2eaa

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IQK Orthosis, Cervical

GMDN Terms

Code Name
45129 Cervical spine collar, single-use

Identifiers

Type ID
Primary 00672736141502

Customer Contacts

Phone
8003210607