Blakesley nasal forceps
- Primary DI
- 04250676715500
- Brand
- Blakesley nasal forceps
- Company
- Spiggle & Theis Medizintechnik GmbH
- Model
- 30-352-00
- Catalog number
- 30-352-00
- Device description
- 45° curved upwards 3.0 mm, WL 130 mm, irrigation channel
- Published
- 2022-09-23
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| LRC | INSTRUMENT, ENT MANUAL SURGICAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LRC | Instrument, Ent Manual Surgical | Ear, Nose, Throat | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04250676715500 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04250676715500 | 04250676715500 | 4250676715500 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical soft-tissue manipulation forceps, alligator, reusable | A long, thin, hand-held manual surgical instrument designed to facilitate grasping and manipulation of soft-tissues/anatomical structures [typically during ear/nose/throat (ENT) surgery]; it is not intended for insertion through an endoscope, nor into the eye, and is not a dedicated biopsy device. Commonly referred to as alligator- or crocodile-forceps, it has a slender body (to allow for restricted access) and small grasping blades which are hinged close to the distal (working) end. It is a metallic device available in various sizes/lengths; some types may include an integrated suction channel. This is a reusable device intended to be sterilized prior to use. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +492206908165 | c.winterschladen@spiggle-theis.com |
Regulatory Flags
- DUNS number
- 332893028
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- true
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