Identity
- Trade Name
- MINILAP FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- MiniGrip Alligator Grasper FDA UDI
- Model / Reference
- IPN002705 FDA UDI
- Description
- MiniGrip Alligator Grasper FDA UDI
Identifiers
- Catalog Number
- PGAC300 FDA UDI
- Primary DI / UDI-DI
- 14026704582607 FDA UDI
- 510(k) Number
- K172775 FDA UDI
- FDA Product Code
- OCW FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 300 Millimeter FDA UDI
Category: Rigid endoscopic tissue manipulation forceps, single-use
Minilap by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Rigid endoscopic tissue manipulation forceps, single-use.
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Cleared under the same submission
K172775 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 5beccbfc-4fb3-486c-ade3-69bf9c220958 37 fields · synced May 31, 2026