Primary Device ID | 20884521013374 |
NIH Device Record Key | 4073439d-d68c-4d49-8ff7-f14861314b96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Monoject |
Version Model Number | 1180100555 |
Catalog Number | 1180100555 |
Company DUNS | 080935429 |
Company Name | Cardinal Health, Inc. |
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 | true |
OTC Over-The-Counter | false |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Total Volume | 1 Milliliter |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521013377 [Primary] |
GS1 | 20884521013374 [Package] Contains: 10884521013377 Package: PACK_OR_INNER_PACK [100 Units] In Commercial Distribution |
GS1 | 30884521013371 [Package] Contains: 10884521013377 Package: CASE [500 Units] In Commercial Distribution |
FMF | Syringe, piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2024-10-31 |
Device Publish Date | 2016-09-24 |
30884527022742 | Insulin Syringe |
30884527022735 | Insulin Syringe |
20884527022721 | Insulin Syringe |
20884527022714 | Insulin Syringe |
00884521169541 | Insulin Syringe |
00884521169527 | Insulin Syringe |
00884521169503 | Insulin Syringe |
20884527022677 | Insulin Syringe |
30884527022667 | Insulin Syringe |
00884521169442 | Insulin Syringe |
10884527022649 | Insulin Syringe |
20884521151847 | Insulin Syringe with Extra Fine Needle |
20884521151830 | Insulin Syringe with Extra Fine Needle |
20884521151823 | Insulin Syringe with Extra Fine Needle |
30884521010431 | Endodontic Needle |
20884521005690 | 0.9% Sodium Chloride,Flush Syringe, 2.5 mL Fill, Blunt Cannula |
10884527017966 | Filter Needle,Aluminum Hub |
20884527006752 | Blood Collection Tube,Silicone Coated Blue Stopper, Buffered Sodium Citrate 0.5 mL 3.2% Solution |
10884527006632 | Blood Collection Tube,Silicone Coated Lavender Stopper, EDTA (K3) 0.05 mL 15.0% Solution, 5 mL D |
10884521163706 | 0.9% Sodium Chloride,Flush Syringe, 2.5 mL Fill |
10884521163690 | 0.9% Sodium Chloride,Flush Syringe, 5 mL Fill |
10884521163683 | 0.9% Sodium Chloride,Flush Syringe, 3 mL Fill |
10884521163676 | 0.9% Sodium Chloride,Flush Syringe, 10 mL Fill |
20884521150093 | Blood Collection Tube,Glycerine Coated Lavender Stopper, EDTA (K3) 0.04 mL 15.0% Solution, 4.0 m |
20884521102757 | Needleless Med Prep Cannula |
20884521102498 | Enteral Syringe with Tip Cap |
20884521082929 | Blunt Tip Cannula,Vial Access Pin |
20884521082493 | Vial Access Cannula,Smart Tip |
10884521082472 | Vial Access Combo,Blunt Tip |
10884521015050 | 1 mL Insulin Syringe,Permanent Needle |
20884521015033 | 1 mL Insulin Syringe,Permanent Needle |
10884521015029 | 1 mL Insulin Syringe,Permanent Needle |
10884521015005 | 3/10 mL Insulin Syringe,Permanent Needle |
10884521014985 | 1/2 mL Insulin Syringe,Permanent Needle |
10884521014923 | 1/2 mL Insulin Syringe,Permanent Needle |
10884521014909 | 1/2 mL Insulin Syringe,Permanent Needle |
10884521014480 | Safety Syringe Tip Cap |
20884521013909 | 1/2 mL Tuberculin Syringe,Permanent Needle |
20884521013077 | Blood Collection/Infusion Set,Female Luer, 12 inch (30.5 cm) Tubing |
20884521012995 | Blood Collection/Infusion Set,Female Luer, 12 inch (30.5 cm) Tubing |
20884521012971 | Blood Collection/Infusion Set,Female Luer, 12 inch (30.5 cm) Tubing |
20884521008790 | Standard Hypodermic Needle,Aluminum Hub |
20884521008752 | Standard Hypodermic Needle,Aluminum Hub |
20884521008745 | Standard Hypodermic Needle,Aluminum Hub |
20884521008707 | Standard Hypodermic Needle,Aluminum Hub |
20884521008646 | Standard Hypodermic Needle,Aluminum Hub |
20884521008585 | Standard Hypodermic Needle,Aluminum Hub |
20884521008547 | Standard Hypodermic Needle,Aluminum Hub |
20884521008431 | Standard Hypodermic Needle,Aluminum Hub |
20884521008387 | Standard Hypodermic Needle,Aluminum Hub |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MONOJECT 74560228 2099750 Dead/Cancelled |
SHERWOOD SERVICES AG 1994-08-08 |
MONOJECT 74191238 1762511 Dead/Cancelled |
Ecolab Inc. 1991-08-05 |
MONOJECT 73569258 1403009 Live/Registered |
SHERWOOD MEDICAL COMPANY 1985-11-18 |
MONOJECT 73569236 1403008 Live/Registered |
SHERWOOD MEDICAL COMPANY 1985-11-18 |
MONOJECT 73170520 1124445 Dead/Cancelled |
SHERWOOD MEDICAL INDUSTRIES INC. 1978-05-15 |
MONOJECT 72037194 0664129 Dead/Expired |
ROEHR PRODUCTS CO., INC. 1957-09-13 |