FDA UDI
In Commercial Distribution
🇺🇸 United States
Pulse® PURE™
DI: 10813172021844
·
Model: 178352
·
INNOVATIVE HEALTHCARE CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
200
Basic Information
- Brand Name
- Pulse® PURE™
- Primary DI
- 10813172021844
- Version / Model
- 178352
- Company Name
- INNOVATIVE HEALTHCARE CORPORATION
- Labeler DUNS
- 802020693
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 200
- Record Status
- Published
- Publish Date
- 2022-12-08
- Public Version
- 1
- Public Version Date
- 2022-12-16
- Public Version Status
- New
- Public Device Record Key
- 59129fa5-eae1-49c6-9561-6a1791925753
Device Description
Gloves, Exam, Nitrile, Non-Sterile, Powder-Free, Textured, Thinfilm, Low Dermatitis Potential, XL
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- 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
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LZA | Polymer Patient Examination Glove | General Hospital | 880.6250 | 1 |
| LZC | Patient Examination Glove, Specialty | General Hospital | 880.6250 | 1 |
| QDO | Fentanyl And Other Opioid Protection Glove | General Hospital | 880.6250 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 56286 | Nitrile examination/treatment glove, non-powdered, non-antimicrobial | A device made of nitrile intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not include antimicrobial agents/materials. The device is used mainly as a two-way barrier to protect patient/staff against contaminants and risk of allergy to latex. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 20813172021841 | GS1 | 200/bx, 10 bx/cs | 10 | In Commercial Distribution | |
| Primary | 10813172021844 | GS1 | ||||
| Unit of Use | 00813172021847 | GS1 |