FDA UDI
In Commercial Distribution
🇺🇸 United States
Sterimed
DI: 00867878000484
·
Model: 3692
·
STERIMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
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Basic Information
- Brand Name
- Sterimed
- Primary DI
- 00867878000484
- Version / Model
- 3692
- Company Name
- STERIMED LLC
- Labeler DUNS
- 080284658
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-12-05
- Public Version
- 5
- Public Version Date
- 2024-09-11
- Public Version Status
- Update
- Public Device Record Key
- f9423058-6aa6-4ef2-932f-17ac9979776d
Device Description
Equipment Cover 36" X 92" W/Tape (3692)
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
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Radiation Sterilization, Ethylene Oxide
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| IZI | System, X-Ray, Angiographic | Radiology | 892.1600 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 12535 | Medical equipment/instrument drape, single-use | A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00867878000484 | GS1 | ||||
| Package | 10867878000481 | GS1 | Inner Pack/Box | 25 | In Commercial Distribution | |
| Package | 20867878000488 | GS1 | Case | 4 | In Commercial Distribution |
Customer Contacts
- Phone
- 770-387-0771
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K853044 | 000 |