FDA UDI
In Commercial Distribution
🇺🇸 United States
Saneck Safety
DI: 00705689017867
·
Model: LEPF-5.5-CR-XL
·
The Cannon Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100
Let the assistant research this device
The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.
Free to try · every answer cites its records
Basic Information
- Brand Name
- Saneck Safety
- Primary DI
- 00705689017867
- Version / Model
- LEPF-5.5-CR-XL
- Company Name
- The Cannon Group, Inc.
- Labeler DUNS
- 131884975
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 100
- Record Status
- Published
- Publish Date
- 2025-02-12
- Public Version
- 1
- Public Version Date
- 2025-02-20
- Public Version Status
- New
- Public Device Record Key
- 204741b1-69f1-4cd4-85c0-4ed59f383f10
Device Description
Extra-Large Latex 5.5MIL Cream Powder-Free Exam Grade Gloves
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
- 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 |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| Package | 00705689017874 | GS1 | Master Carton | 10 | In Commercial Distribution | |
| Primary | 00705689017867 | GS1 | ||||
| Unit of Use | 10705689017864 | GS1 |