FDA UDI
In Commercial Distribution
🇺🇸 United States
23GA Membrane Scraper
DI: 00632307002274
·
Model: 1290.S23-00
·
PEREGRINE SURGICAL, LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- 23GA Membrane Scraper
- Primary DI
- 00632307002274
- Version / Model
- 1290.S23-00
- Company Name
- PEREGRINE SURGICAL, LTD.
- Labeler DUNS
- 622467348
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-05-10
- Public Version
- 1
- Public Version Date
- 2023-05-18
- Public Version Status
- New
- Public Device Record Key
- 75b41c17-d18e-4283-8f56-a70808ef05db
Device Description
23GA Membrane Scraper
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- 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
- Yes
- PM Exempt
- Yes
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Ethylene Oxide
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | General, Plastic Surgery | 878.4800 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 63432 | Epiretinal/inner limiting membrane scraper, single-use | A hand-held manual surgical instrument intended to be used during posterior segment surgery to lift the inner limiting membrane (ILM) and/or an epiretinal membrane (ERM), and which may have additional posterior segment membrane manipulation uses. It includes a dedicated textured tip (e.g., diamond-dusted polymer) intended to effectively grip/lift the membrane for further manipulation (e.g., with forceps); it may additionally include non-powered features (e.g., fibreoptics) to allow cold light to be directed to the surgical site. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00632307002274 | GS1 | ||||
| Package | 10632307002271 | GS1 | Box | 10 | In Commercial Distribution |
Customer Contacts
- Phone
- +1(215)348-0456
- [email protected]
- Phone
- +1(215)348-0456
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 23 Gauge Needle | ||
| Needle Gauge | 23 | Gauge |