Identity
- Trade Name
- Apellis Injection Kit FDA UDI
- Generic Name
- Ophthalmic needle, single-use FDA UDI
- Device Name
- Intravitreal Injection Kit with filter needle and injection needle FDA UDI
- Model / Reference
- IVT-KIT-29G FDA UDI
- Description
- Intravitreal Injection Kit with filter needle and injection needle FDA UDI
Identifiers
- Catalog Number
- IVT-KIT-29G FDA UDI
- Primary DI / UDI-DI
- 00860008043672 FDA UDI
- 510(k) Number
- K222681 FDA UDI
- FDA Product Code
- FMI FDA UDIGAA FDA UDI
- GMDN Term
- Ophthalmic needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 FDA UDI878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
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
- Needle Gauge — 29 Gauge FDA UDILength — .5 Inch FDA UDI
Category: Ophthalmic needle, single-use
Apellis Injection Kit by Altaviz, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic needle, single-use.
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- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Walcott Rx Products — Psi/Eye-Ko, 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 |
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Manufacturer
- Manufacturer
- Altaviz, LLC
Sources (1)
- FDA UDI 896ff276-0455-4d6b-9432-71398aab2e9d 36 fields · synced May 30, 2026