Identity
- Trade Name
- Integra® Jarit® FDA UDI
- Generic Name
- Periocular/lacrimal retractor, hand-held, reusable FDA UDI
- Device Name
- Integra® Jarit® Jaeger Lid Plate, 4-3/8", Double-Ended, Blades 21mm and 24mm, 1.25mm Thickness FDA UDI
- Model / Reference
- X29231 FDA UDI
- Description
- Integra® Jarit® Jaeger Lid Plate, 4-3/8", Double-Ended, Blades 21mm and 24mm, 1.25mm Thickness FDA UDI
Identifiers
- Catalog Number
- X29231 FDA UDI
- Primary DI / UDI-DI
- 10381780404927 FDA UDI
- FDA Product Code
- HOY FDA UDIHNI FDA UDI
- GMDN Term
- Periocular/lacrimal retractor, hand-held, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4750 FDA UDI886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 24 Millimeter FDA UDILength — 21 Millimeter FDA UDI
Category: Periocular/lacrimal retractor, hand-held, reusable
Integra® Jarit® by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI d4e2e68f-59fc-4e9b-9007-d9b8baa84e7e 36 fields · synced Jun 9, 2026