FDA UDI
In Commercial Distribution
🇺🇸 United States
meijer
DI: 00713733229203
·
Model: 713733229203
·
MEIJER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5
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Basic Information
- Brand Name
- meijer
- Primary DI
- 00713733229203
- Version / Model
- 713733229203
- Catalog Number
- 4300495
- Company Name
- MEIJER, INC.
- Labeler DUNS
- 006959555
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 5
- Record Status
- Published
- Publish Date
- 2019-06-28
- Public Version
- 1
- Public Version Date
- 2019-07-08
- Public Version Status
- New
- Public Device Record Key
- d0d02249-d1d3-4825-a394-82f1acef7027
Device Description
Extreme Hydrocolloid blister cushion, all one size, 42 mm x 68 mm
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- 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
- Yes
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NAD | Dressing, Wound, Occlusive | General, Plastic Surgery | 878.4020 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 62873 | Exudate-absorbent dressing, hydrophilic-gel, non-sterile | A non-sterile adhesive covering intended to assist treatment and protection of fluid-filled superficial lesions (e.g., cold sores, mild acne spots/pimples, opened blisters) and/or minor abrasions by producing a water-absorbent gel upon contact with exudate and maintaining a moist environment; it does not contain an antimicrobial agent. It may be available in various forms (e.g., flat sheet/film, pad) and is typically made of hydrocolloid. It is normally available [non-prescription] over-the-counter (OTC). After application, this device cannot be reused. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 10713733229200 | GS1 | case | 24 | In Commercial Distribution | |
| Primary | 00713733229203 | GS1 | ||||
| Unit of Use | 60713733229205 | GS1 |