FDA UDI In Commercial Distribution 🇺🇸 United States

TBL-ABI

DI: B322C0011 · Model: C001 · LD TECHNOLOGY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TBL-ABI
Primary DI
B322C0011
Version / Model
C001
Company Name
LD TECHNOLOGY, LLC
Labeler DUNS
079443785
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-16
Public Version
2
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
d2d62463-6ef5-435b-bb28-d9bd607feb25

Device Description

The TBL-ABI is indicated for use on adult subjects at risk of having or developing peripheral arterial disease (PAD). TBL-ABI is intended for the rapid measurement of ankle-brachial pressure index (ABPI), or ankle-brachial index (ABI), and pulse volume recording (PVR) / volume plethysmography in adults. It is suitable for use in wound care assessment, for assessing symptomatic PAD, and as a screening device for PAD. It may also be used on patients with venous or arterial ulcers prior to the application of compression therapy. TBL-ABI can be used on patients with unilateral lower limb amputation.

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

GMDN Terms

Code Name
16174 Manual-inflation electronic sphygmomanometer, non-portable

Identifiers

Type ID
Primary B322C0011

Customer Contacts

Phone
305-379-9900

Premarket Submissions

Submission Number Supplement Number
K173696 000