Primary Device ID | 04710636640162 |
NIH Device Record Key | 3c8a8566-4341-4efd-a9ab-606bc4fb55c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TD-THIN Sterile Lancets (100pcs/box) |
Version Model Number | TD-5084 |
Company DUNS | 658530993 |
Company Name | TAIDOC TECHNOLOGY CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04710636640162 [Primary] |
QRK | Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature |
Steralize Prior To Use | true |
Device Is Sterile | true |
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
[04710636640162]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-08 |
Device Publish Date | 2023-08-31 |
04710636640162 - TD-THIN Sterile Lancets (100pcs/box) | 2023-09-08 |
04710636640162 - TD-THIN Sterile Lancets (100pcs/box) | 2023-09-08 |
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