Identity
- Trade Name
- Dampening Chamber with Infusion Restrictor Tube FDA UDI
- Generic Name
- Arthroscopic shaver system, electrically-powered FDA UDI
- Model / Reference
- DCIT-RT FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00627825000482 FDA UDI
- FDA Product Code
- FEN FDA UDI
- GMDN Term
- Arthroscopic shaver system, electrically-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1620 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Category: Arthroscopic shaver system, electrically-powered
Dampening Chamber with Infusion Restrictor Tube by Laborie Medical Technologies Canada ULC — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Arthroscopic shaver system, electrically-powered.
- Shrill® — JOIMAX, INC. · Class I
- Formula — Stryker Corp. · Class I
- Formula — Stryker Corp. · Class I
- Formula — Stryker Corp. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- FMS — Medos International Sàrl · Class II
- Arthrex® — Arthrex, Inc. · Class I
- Shaver blades — JOIMAX, INC. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Laborie Medical Technologies Canada ULC
Sources (1)
- FDA UDI 1d60e05b-e04f-40d5-94f5-319d362a9668 32 fields · synced May 31, 2026