FDA UDI
In Commercial Distribution
🇺🇸 United States
LMA
DI: 05060112313202
·
Model: IPN046396
·
TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- LMA
- Primary DI
- 05060112313202
- Version / Model
- IPN046396
- Catalog Number
- MAD700
- Company Name
- TELEFLEX INCORPORATED
- Labeler DUNS
- 002348191
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-16
- Public Version
- 4
- Public Version Date
- 2019-10-17
- Public Version Status
- Update
- Public Device Record Key
- bce3a0ea-85f3-4643-8396-26d315879403
Device Description
Laringo-Tracheal Mucosal Atomatization Device without Syringe
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
- 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
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| CCT | APPLICATOR (LARYNGO-TRACHEAL), TOPICAL ANESTHESIA | Anesthesiology | 868.5170 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 31343 | Laryngotracheal anaesthesia applicator | A non-sterile container (e.g., a spray bottle) that is prefilled with an anaesthetic agent and intended to be used to apply the agent to the oropharynx and upper airway, to relax laryngotracheal reflexes prior to an intervention [typically insertion of an endotracheal (ET) tube or other type of tracheal tube]. It is typically used on non-pharmacologically paralyzed patients where multiple reflexes (e.g., the gag reflex, glottic closure, vocal cord spasm, cough reflex, and bronchoconstriction) could make difficult or inhibit safe intervention. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 15060112313209 | GS1 | Box | 25 | Not in Commercial Distribution | 2019-09-30 |
| Primary | 05060112313202 | GS1 | ||||
| Package | 25060112313206 | GS1 | Case | 4 | Not in Commercial Distribution | 2019-09-30 |
Customer Contacts
- Phone
- +1(919)544-8000
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K153470 | 000 |