FDA UDI
In Commercial Distribution
🇺🇸 United States
Health-Tec/DHP Pro-Tec Latex Exam Gloves
DI: D773410PPFM21
·
Model: 410-PPFM2
·
Dental Health Products Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Health-Tec/DHP Pro-Tec Latex Exam Gloves
- Primary DI
- D773410PPFM21
- Version / Model
- 410-PPFM2
- Catalog Number
- 410-PPFM2
- Company Name
- Dental Health Products Inc
- Labeler DUNS
- 623191194
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2022-09-21
- Public Version
- 1
- Public Version Date
- 2022-09-29
- Public Version Status
- New
- Public Device Record Key
- c32b7798-df18-4ee6-b37a-a7f4c96a849f
Device Description
Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size Medium 100/box
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- Yes
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LYY | Latex Patient Examination Glove | General Hospital | 880.6250 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47172 | Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial | A device made of Hevea natural rubber latex (NRL) 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 both the patient and the staff against various contamination. It will have appropriate characteristics regarding tactility/comfort of use, and should provide appropriate physical properties (e.g., strength, elasticity), and uniformity of dimensions. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | D773410PPFM21 | HIBCC |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K000999 | 000 |