Identity
- Trade Name
- Anaesthetic Needles FDA UDI
- Generic Name
- Ophthalmic needle, single-use FDA UDI
- Device Name
- 25g x 1 1/4" Peribulbar FDA UDI
- Model / Reference
- 0642-03/Y FDA UDI
- Description
- 25g x 1 1/4" Peribulbar FDA UDI
Identifiers
- Catalog Number
- M0642 FDA UDI
- Primary DI / UDI-DI
- 05056030400162 FDA UDI
- FDA Product Code
- MED FDA UDI
- GMDN Term
- Ophthalmic needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6885 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Ophthalmic needle, single-use
Anaesthetic Needles by Sterimedix Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Walcott Rx Products — Psi/Eye-Ko, Inc. · Class I
- Anodyne Surgical — 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
- Sterimedix Limited
Sources (1)
- FDA UDI 72d2d6f0-f6ec-4177-b3e4-d44aabecab38 34 fields · synced Jun 8, 2026