Identity
- Trade Name
- MiniLap Percutaneous Surgical System, Babcock Grasper EUDAMEDMINILAP FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- MiniLap Graspers, various types EUDAMEDClutch Grasper FDA UDI
- Model / Reference
- CLC250 EUDAMEDIPN922567 FDA UDI
- Description
- Clutch Grasper FDA UDI
Identifiers
- Catalog Number
- CLC250 FDA UDI
- Primary DI / UDI-DI
- 14026704737960 EUDAMEDFDA UDI
- Basic UDI-DI
- 08019020000000000000129KM EUDAMED
- 510(k) Number
- K070686 FDA UDI
- FDA Product Code
- OCW FDA UDI
- EMDN Code
- K01020104 MINIMALLY INVASIVE SURGERY FORCEPS, SINGLE-USE EUDAMED
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Dimensions & Sizes
- Size
- Length — 250 Millimeter FDA UDI
Category: Rigid endoscopic tissue manipulation forceps, single-use
Minilap by Teleflex Incorporated — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic tissue manipulation forceps, single-use.
- Standard Clamp Disposable SCD22-1 — Standard Bariatrics · Class II
- Direct Drive Reposable Graspers — APPLIED MEDICAL RESOURCES CORP. · Class I
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- ReNew — MICROLINE SURGICAL, INC. · Class II
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Cleared under the same submission
K070686 also covers:
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
- MINILAP — TELEFLEX INCORPORATED
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (2)
- FDA UDI b75c9ecf-f405-46fa-9ca9-5d4c9a0dbcc1 37 fields · synced Jul 15, 2026
- EUDAMED ca62af03-fad3-4567-82e1-1e084e6c5455 61 fields · synced Jul 15, 2026